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All Clinical Trials
A listing of 23115 clinical trials actively recruiting volunteers for paid trials and research studies in various therapeutic areas.
23005 - 23016 of 23115
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 Trial
Buy Retatrutide Online Through Celia
Recruiting
Retatrutide (formerly M25) is an investigational peptide being studied for its potential in supporting weight management and metabolic health. It acts on GLP-1, GIP, and glucagon receptors to influence appetite, energy regulation, and fat metabolism.
Conditions:
Healthy
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Semaglutide and Tirzepatide are advanced GLP-1 medications designed to support weight management and metabolic health. They work by targeting GLP-1 receptors in the body, helping regulate appetite, improve blood sugar control, and support sustainable weight loss (up to 22% of body weight).
Get $50 off your first order using promo code: policy-lab-50
Conditions:
Overweight
Overweight and Obesity
Obesity
Weight Loss
Morbid Obesity
Featured Trial
Birth Control Clinical Research Study
Recruiting
Living with obesity and looking for a birth control option that is right for you? Clinical trials are now enrolling women with a body mass index (BMI) of 30 or more in the area to help study a potential new progestin-only contraceptive patch. Participating in research studies can help advance birth control options. Don’t let financial stress hold you back. All study-related assessments, care, and study patch are available at no cost. You may also be reimbursed for study-related travel.
Conditions:
Obesity
Overweight
Overweight and Obesity
Featured Trial
Depression Clinical Trial
Recruiting
Join us in researching a potential investigational treatment for Depression. Reimbursement for study-related expenses may be available to you.
Qualifying participants:
•Are between 18-65
•Have been experiencing a major depressive episode for at least a month
Qualifying participants:
•Are between 18-65
•Have been experiencing a major depressive episode for at least a month
Conditions:
Depression
Major Depressive Disorder
Depressive Disorder
Depressive Symptoms
Depressive Disorder
Featured Offer
Ketamine Therapy—At Home, Clinician-Guided (Innerwell)
If you’re exploring options besides a clinical trial, Innerwell provides at-home ketamine therapy with medical oversight and structured support. Ketamine-assisted treatment may help “reset” rigid stress and mood patterns, and some people feel relief within a few sessions. Your care team works with you to tailor treatment and track progress every step of the way. Proven effective for Anxiety, PTSD, Depression, Addiction, and other disease areas.
Conditions:
Anxiety
Anxiety Disorders
Generalized Anxiety Disorder
Depression
Depression
Objective Measures of Nerve Integrity, Posture, Gait and Blood Flow, After Nerve Decompression
Recruiting
The purpose of this study is to measure the effect of nerve decompression on the recovery of the treated nerves. To obtain objective data during surgery of the treated nerves' via electrical signals and muscle power when stimulated. Also, to monitor muscle strength, balance/gait and blood flow in the lower extremity before and after surgery.
Gender:
ALL
Ages:
Between 18 years and 85 years
Trial Updated:
02/15/2021
Locations: Anderson Podiatry Center, Neuropathy Testing Center of Colorado, Fort Collins, Colorado
Conditions: Diabetic Peripheral Neuropathy
Phase 2 Safety and Immunogenicity Study of Rift Valley Fever Vaccine
Recruiting
This study is to collect safety and immunogenicity data for an Rift Valley Fever (RVF) vaccine
Gender:
ALL
Ages:
Between 18 years and 65 years
Trial Updated:
02/10/2021
Locations: Special Immunization Program, Division of Medicine, USAMRIID, Fort Deterick, Maryland
Conditions: Rift Valley Fever
Virtual Reality During Pediatric Cast Removal
Recruiting
This study is a randomized control trial of Virtual Reality during cast removal procedures at a pediatric tertiary care center.
Gender:
ALL
Ages:
Between 4 years and 12 years
Trial Updated:
02/10/2021
Locations: Gillette Children's Specialty Healthcare, Saint Paul, Minnesota
Conditions: Fractures, Bone
Comparison of Toxicities Between Proton Therapy and IMRT for Post Operative Treatment of Endometrial or Cervical Cancers.
Recruiting
This trial is designed as a non-randomized pilot trial to study, in a preliminary fashion, whether proton radiation therapy (proton RT) reduces acute gastrointestinal toxicities at the end of treatment compared to intensity modulated radiation therapy (IMRT)
Gender:
Female
Ages:
18 years and above
Trial Updated:
02/08/2021
Locations: Mayo Clinic in Rochester, Rochester, Minnesota
Conditions: Cervical Cancer, Endometrial Cancer
Safety and Efficacy of Endoscopic Assisted Push Gastrostomy Using Gastrostomy Technique
Recruiting
Most pediatric gastroenterologists use an endoscopic pull technique to place gastrostomy tubes. We assessed an endoscopic gastropexy technique for gastrostomy tube placement that allows immediate placement of a low profile gastrostomy tube or gastro-jejunostomy tube. The procedure involves endoscopy with the placement of three T-fasteners that are placed through the skin into the stomach, placating and securing the stomach to the abdominal wall. This attachment process promotes formation of a st... Read More
Gender:
ALL
Ages:
17 years and below
Trial Updated:
01/26/2021
Locations: The Children's Hospital of San Antonio, San Antonio, Texas
Conditions: Gastrostomy, Gastrostomy Complications, Gastrostomy Tube Site Complication, Pain, Postoperative
Ambulatory Surgical Center Implantable Cardioverter-Defibrillator Outcomes Registry
Recruiting
The primary objectives for the registry is to evaluate the overall incidence of serious complications or adverse events for primary implants and replacement devices, and assess the cost and time efficiency for both physicians and patients. The Registry is a multi ASC data collection registry. Data collection will occur at the time of screening, implant, and 2 weeks after implant at the time of wound check.
Gender:
ALL
Ages:
All
Trial Updated:
01/20/2021
Locations: Cardio Surgical Partners, LLC, Lehi, Utah
Conditions: Arrhythmia
An Active and Placebo-Controlled Study of Brazikumab in Participants With Moderately to Severely Active Ulcerative Colitis
Recruiting
The present study D5272C00001 (Legacy # 3151-201-008) seeks to evaluate the efficacy and safety of brazikumab versus placebo in patients with moderately to severely active UC and will include assessments of clinical responses as demonstrated by improvement of symptoms and of colonic mucosal appearance as observed on endoscopy.
Gender:
All
Ages:
Between 18 years and 80 years
Trial Updated:
01/19/2021
Locations: Research Site, Tucson, Arizona +79 locations
Conditions: Ulcerative Colitis
Microsurfaced Grafts in Deep Burn Wounds
Recruiting
This study is designed as a prospective, randomized, within subject controlled design to evaluate the effectiveness of Microsurfaced vs Control cadaveric grafts for coverage of acute deep-partial or full-thickness burn wounds to promote wound healing. This study will be performed in 2 parts: Time to wound bed preparedness through 6 weeks (Part A) and wound site healing, graft take and long-term scar outcomes (Part B). Subjects will be treated with both control and microsurfaced cadaveric grafts... Read More
Gender:
ALL
Ages:
21 years and above
Trial Updated:
01/13/2021
Locations: Joseph M Still Research Foundation, Augusta, Georgia
Conditions: Burns, Wound Heal
Comparison Of Radiation Exposure To Patients During Endoscopic Retrograde Cholangiopancreatography (ERCP) Performed By Endoscopists Trained In Judicious Use Of Fluoroscopy With Those Without Formal Training
Recruiting
Purpose: To compare the radiation exposure in patients during Endoscopic retrograde cholangiopancreatography (ERCP) done by Endoscopists formally trained in judicious use of fluoroscopy versus ERCPs done by Endoscopists without such formal training.
Research design: This is an observational study to compare radiation exposure in patients during ERCPs based on formal training.
Procedures to be used: None Risks and potential benefits There are no risks associated with this study as it is a retro... Read More
Gender:
ALL
Ages:
Between 18 years and 100 years
Trial Updated:
01/11/2021
Locations: Memorial Hermann Hospital, Houston, Texas
Conditions: Pancreatic Cancer
Talazoparib, an Oral PARP Inhibitor, in Patients With Advanced Solid Tumors and Aberrations in Genes Involved in DNA Damage Response
Recruiting
Background:
People with advanced cancer are usually treated with surgery, radiation, immunotherapy drugs, or chemotherapy drugs. Talazoparib is a type of drug called a PARP inhibitor. It prevents DNA repair and has shown anticancer activity in early clinical trials. Researchers want to learn more about how it works in different types of patients.
Objective:
To find out how talazoparib works in tumor cells and if it works differently in people who have or have not already been treated with ano... Read More
Gender:
All
Ages:
18 years and above
Trial Updated:
01/09/2021
Locations: National Institutes of Health Clinical Center, Bethesda, Maryland
Conditions: Solid Tumors
Trigger Point Injection for Myofascial Pain Syndrome in the Low Back: A Randomized Controlled Trial
Recruiting
Rationale: Low back pain (LBP), or myofascial pain syndrome (MPS) of the low back, accounts for approximately 2.63 million visits in the United States, or 2.3 percent of annual Emergency Department (ED) visits. An estimated 100 billion dollars per year is lost from LBP. Approximately one-third of this is direct costs. Previous studies have established the safety of trigger point injections (TPI). However, the results of these studies are highly heterogeneous regarding TPI's ability to treat pain... Read More
Gender:
ALL
Ages:
18 years and above
Trial Updated:
01/09/2021
Locations: Department of Emergency Medicine, Madigan Army Medical Center, Tacoma, Washington
Conditions: Low Back Pain, Myofascial Pain Syndrome Lower Back
Latency Antibiotics in Previable PPROM, 18 0/7- 22 6/7 WGA
Recruiting
This study is a non-blinded, prospective, randomized controlled trial designed to compare the effect of outpatient oral antibiotics (i.e., amoxicillin and azithromycin) on the length of time (days) that pregnancy continues after a patient's water bag has ruptured prematurely. If a patient has been diagnosed with rupture of their water bag between 18 0/7 weeks and 22 6/7 weeks and there are no other associated complications with the pregnancy, the patient is eligible for initial consideration for... Read More
Gender:
FEMALE
Ages:
18 years and above
Trial Updated:
01/07/2021
Locations: Woman's Hospital, Baton Rouge, Louisiana
Conditions: Rupture of Membranes; Delayed Delivery (Following Spontaneous Rupture), Rupture of Membranes; Premature, Rupture of Membranes; Premature, Affecting Fetus, Preterm Birth, Preterm PROM (Pregnancy), Preterm Labor
23005 - 23016 of 23115
