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                    Oregon Paid Clinical Trials
A listing of 1212  clinical trials  in Oregon  actively recruiting volunteers for paid trials and research studies in various therapeutic areas.
            1141 - 1152 of 1212
        
                Oregon is currently home to 1212 active clinical trials, seeking participants for engagement in research studies. These trials take place at a variety of cities in the state, including Portland, Eugene, Medford and Clackamas. Whether you're a healthy volunteer interested in paid medical research or someone seeking trials related to a specific condition, the state offers a diverse array of opportunities in your vicinity.
            
                                                Featured Trial
                
                Healthy Participants Needed (Colonoscopy + Cancer Screening)
            
        Recruiting
            
        Earn $325 - $475 in electronic payment card compensation for your time and effort by participating in a clinical study to develop a blood test that may one day help screen for colon cancer. Take a quick quiz to see if you qualify.
    
    
                            Conditions: 
                                    
        
            
                        Healthy
                    
                                    
                        Healthy Volunteers
                    
                                    
                        Healthy Subjects
                    
                                    
                        Healthy Volunteer
                    
                                    
                        Healthy Participants
                    
                                    Featured Offer
                
                Lose Weight with GLP-1 Medications
            
        Recruiting
            
        Policy Lab has partnered with OnlineSemaglutide.org to offer trusted access to semaglutide and other GLP-1 medications, including generic alternatives to Ozempic® and Wegovy®. 
GLP-1 medications are scientifically backed to help individuals achieve significant weight loss—on average, 15-20% of body weight within a year.
As a valued user, you’re eligible for $50 off your first program with code policy-lab-50.
    GLP-1 medications are scientifically backed to help individuals achieve significant weight loss—on average, 15-20% of body weight within a year.
As a valued user, you’re eligible for $50 off your first program with code policy-lab-50.
                            Conditions: 
                                    
        
            
                        Overweight
                    
                                    
                        Overweight and Obesity
                    
                                    
                        Obesity
                    
                                    
                        Weight Loss
                    
                                    
                        Morbid Obesity
                    
                                    Featured Trial
                
                Stroke Clinical Study
            
        Recruiting
            
        A clinical study for people that suffer with Stroke
    
    
                            Conditions: 
                                    
        
            
                        Stroke
                    
                                    Featured Trial
                
                Chronic Kidney Disease (CKD) Clinical Study
            
        Recruiting
            
        A clinical study for people that suffer with Chronic Kidney Disease (CKD)
    
    
                            Conditions: 
                                    
        
            
                        Chronic Kidney Disease (CKD)
                    
                                    Featured Trial
                
                Ischemic heart disease (IHD) Clinical Study
            
        Recruiting
            
        A clinical study for people that suffer with Ischemic heart disease (IHD)
    
    
                            Conditions: 
                                    
        
            
                        Ischemic heart disease (IHD)
                    
                                    
                
                                    Brown Adipose Tissue Activation by Spinal Cord Stimulation
                                
            
            
        Recruiting
                            
            
                The objective of this study is to investigate and utilize spinal cord stimulation (SCS) as an effective approach to eliciting weight loss and potentially alleviating Type 2 diabetes mellitus (DM), as evidenced by increasing metabolism of adipose tissue.             
        
        
    Gender:
                ALL
            Ages:
                Between 21 years and 70 years
            Trial Updated:
                04/01/2024
            
            Locations: Oregon Health & Science University, Portland, Oregon         
        
        
            Conditions: Pain, Back, Obesity, Morbid, Type 2 Diabetes
        
            
        
    
                
                                    Lovenox 30 mg Twice Daily (BID) Versus 40 mg Once Daily (QD)
                                
            
            
        Recruiting
                            
            
                The risk of developing a blood clot occurs in up to 60% of all critical care patients. Many times enoxaparin (or Lovenox) is given to patients who are at a higher risk of developing clots in their legs or lungs. There are two standard doses of enoxaparin that are recommended by the drug companies. These two doses have never been directly compared in trauma, general, and vascular surgery patients. The purposes of this study are:
1. to compare the development of blood clots in patients receiving...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 15 years and 100 years
            Trial Updated:
                04/01/2024
            
            Locations: Oregon Health & Science University, Portland, Oregon         
        
        
            Conditions: Trauma, Surgery, Deep Vein Thrombosis (DVT), Thromboembolic Events
        
            
        
    
                
                                    Collaboration Oriented Approach to Controlling High Blood Pressure
                                
            
            
        Recruiting
                            
            
                Hypertension is a significant contributor to poor cardiovascular outcomes. Self-management support tools can increase patient behaviors to improve blood pressure. The investigators created a clinical decision support app, called COACH, to integrate home blood pressure data and goals into EHR reporting and workflow with communications informed by behavioral economics principles to support shared decision-making. The study aims to measure the effectiveness of the COACH intervention in a pragmatic...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 100 years
            Trial Updated:
                03/22/2024
            
            Locations: Oregon Health & Science University, Portland, Oregon         
        
        
            Conditions: Hypertension, Multiple Chronic Conditions
        
            
        
    
                
                                    Carrying for the Culture
                                
            
            
        Recruiting
                            
            
                Suboptimal postpartum health outcomes in the US, including low rates of lactation and high rates of postpartum depression, contribute to high rates of perinatal mortality and morbidity as well as long-term and intergenerational health outcomes. Black birthing parents and infants are at the highest risk, with the lowest rates of lactation and the highest rates of postpartum depression. Yet most interventions to support lactation and postpartum mental health are based on models of care that are un...  Read More             
        
        
    Gender:
                FEMALE
            Ages:
                18 years and above
            Trial Updated:
                03/20/2024
            
            Locations: Nurturely, Eugene, Oregon         
        
        
            Conditions: Postpartum Depression, Breast Feeding
        
            
        
    
                
                                    Ripasudil for Enhanced Corneal Clearing Following Descemet Membrane Endothelial Keratoplasty in Fuchs' Dystrophy
                                
            
            
        Recruiting
                            
            
                Recently, published literature has reported that performing a descemetorhexis in combination with topical Rho kinase (ROCK) inhibitor therapy was successful in clearing edematous corneas in patients with Fuchs Endothelial Corneal Dystrophy.
Ripasudil hydrochloride hydrate( Glanatec ophthalmic solution 0.4%), a potent ROCK inhibitor, has been approved in Japan since 2014 for ocular use in the treatment of glaucoma. Ripasudil acts as an IOP-lowering drug by affecting aqueous outflow through the t...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 30 years and 99 years
            Trial Updated:
                03/19/2024
            
            Locations: Devers Eye Institute, Portland, Oregon         
        
        
            Conditions: Fuchs Endothelial Dystrophy
        
            
        
    
                
                                    A Study of TSR-022 in Participants With Advanced Solid Tumors (AMBER)
                                
            
            
        Recruiting
                            
            
                This is a first-in-human study evaluating the anti-T cell immunoglobulin and mucin containing protein-3 (TIM-3) antibody TSR-022. The study will be conducted in 2 parts with Part 1 consisting of dose escalation and Part 2 dose expansion. Part 1 will determine the recommended Phase 2 dose (RP2D) of TSR-022 and Part 2 will evaluate the antitumor activity of TSR-022 in combination with TSR-042 or docetaxel and as monotherapy.             
        
        
    Gender:
                All
            Ages:
                18 years and above
            Trial Updated:
                03/14/2024
            
            Locations: GSK Investigational Site, Eugene, Oregon         
        
        
            Conditions: Neoplasms
        
            
        
    
                
                                    Evaluation of the PrevisEA Device for Predicting Gastrointestinal Impairment
                                
            
            
        Recruiting
                            
            
                PrevisEA is a noninvasive, disposable device that uses audio spectral analysis of sounds produced by the gastrointestinal tract to predict gastrointestinal impairment (GII). GII is most commonly associated with postoperative ileus (POI), but could be the result of other causes, such as early postoperative bowel obstruction. GII is defined as failure of successful early oral re-feeding in a subject undergoing major abdominal surgery. For subjects who are allowed to resume a diet during the first...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 90 years
            Trial Updated:
                03/11/2024
            
            Locations: Oregon Health and Science University, Portland, Oregon         
        
        
            Conditions: Gastrointestinal Complication
        
            
        
    
                
                                    KEEP Connecting Kin
                                
            
            
        Recruiting
                            
            
                The current study provides a unique opportunity to conduct a summative evaluation of the KEEP Connecting Kin (KEEP-CK) program by leveraging extant relationships with Oregon's Child Welfare System (CWS), Self-Sufficiency Program (SSP), and our community partners to address the needs of informal kinship families and the youth in their care. Specifically, a randomized "services-as-usual" (SAU) waitlist control design plus qualitative methods will be used to evaluate the immediate (post-interventio...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 4 years and 18 years
            Trial Updated:
                02/27/2024
            
            Locations: Oregon Center Learning Center, Eugene, Oregon         
        
        
            Conditions: Internalizing Behavior, Externalizing Behavior, Child Permanency, Parenting, Parent Stress, Service Utilization
        
            
        
    
                
                                    Enroll -HD: A Prospective Registry Study in a Global Huntington's Disease Cohort
                                
            
            
        Recruiting
                            
            
                Enroll-HD is a longitudinal, observational, multinational study that integrates two former Huntington's disease (HD) registries-REGISTRY in Europe, and COHORT in North America and Australasia-while also expanding to include sites in Latin America. More than 30,000 participants have now enrolled into the study. With annual assessments and no end date, Enroll-HD has built a large and rich database of longitudinal clinical data and biospecimens that form the basis for studies developing tools and b...  Read More             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                02/26/2024
            
            Locations: Oregon Health and Science University, Portland, Oregon         
        
        
            Conditions: Huntington's Disease
        
            
        
    
                
                                    OCT in Diagnosis of Irregular Corneas
                                
            
            
        Recruiting
                            
            
                This main goal of this study is to improve the detection, classification, monitoring, and treatment of irregular corneas due to keratoconus, warpage, dry eye, scar, stromal dystrophies, and other corneal conditions.
The primary goal will be achieved by using optical coherence tomography (OCT) to:
1. Develop an OCT-based system to classify and evaluate corneal-shape irregularities.
2. Develop OCT metrics for more sensitive detection of keratoconus progression.
3. Develop OCT-and-topography guid...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 14 years and 85 years
            Trial Updated:
                02/20/2024
            
            Locations: Humberto Martinez, Portland, Oregon         
        
        
            Conditions: Keratoconus, Corneal Opacity, Corneal Dystrophy
        
            
        
    
                
                                    cfDNA Assay Prospective Observational Validation for Early Cancer Detection and Minimal Residual Disease
                                
            
            
        Recruiting
                            
            
                This is an observational case-control study to train and validate a genome-wide methylome enrichment platform to detect multiple cancer types and to differentiate amongst cancer types. The cancers included in this study are brain, breast, bladder, cervical, colorectal, endometrial, esophageal, gastric, head and neck, hepatobiliary, leukemia, lung, lymphoma, multiple myeloma, ovarian, pancreatic, prostate, renal, sarcoma, and thyroid. These cancers were selected based on their prevalence and mort...  Read More             
        
        
    Gender:
                ALL
            Ages:
                40 years and above
            Trial Updated:
                02/15/2024
            
            Locations: Oregon Health Sciences University, Portland, Oregon         
        
        
            Conditions: Brain Cancer, Breast Cancer, Bladder Cancer, Cervical Cancer, Colorectal Cancer, Endometrial Cancer, Esophageal Cancer, Stomach Cancer, Head and Neck Cancer, Hepatobiliary Cancer, Leukemia, Lung Cancer, Lymphoma, Multiple Myeloma, Ovarian Cancer, Pancreatic Cancer, Prostate Cancer, Renal Cancer, Sarcoma, Thyroid Cancer
        
            
        
    
                
                                    Longitudinal Study of Urea Cycle Disorders
                                
            
            
        Recruiting
                            
            
                Urea cycle disorders (UCD) are a group of rare inherited metabolism disorders. Infants and children with UCD commonly experience episodes of vomiting, lethargy, and coma. The purpose of this study is to perform a long-term analysis of a large group of individuals with various UCDs. The study will focus on the natural history, disease progression, treatment, and outcome of individuals with UCD.             
        
        
    Gender:
                ALL
            Ages:
                All
            Trial Updated:
                02/10/2024
            
            Locations: Oregon Health and Science University, Portland, Oregon         
        
        
            Conditions: Brain Diseases, Metabolic, Inborn, Amino Acid Metabolism, Inborn Errors, Urea Cycle Disorders
        
            
        
    