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Norfolk, VA Paid Clinical Trials
A listing of 334 clinical trials in Norfolk, VA actively recruiting volunteers for paid trials and research studies in various therapeutic areas.
325 - 334 of 334
There are currently 334 clinical trials in Norfolk, Virginia looking for participants to engage in research studies. Trials are conducted at various facilities, including Children's Hospital of The King's Daughters, Sentara Norfolk General Hospital, Virginia Oncology Associates and Eastern Virginia Medical School. Whether you're a healthy volunteer looking to participate in paid medical research or seeking trials related to a specific condition, the city provides a diverse range of opportunities near you.
Featured Trial
Paid Clinical Studies Nationwide
Recruiting
Nationwide clinical trials offered in your area. Some trials offering up to several thousand dollars in compensation for participation.
Featured Trial
Chronic Cough Clinical Study
Recruiting
We are evaluating an investigational treatment to see if it may help people dealing with chronic cough.
Eligible participants will receive study-related medical care at no cost. You may be compensated for study-related travel and time. Health insurance is not required. If you qualify, you may receive:
Payment up to $1500, which varies by study.
Eligible participants will receive study-related medical care at no cost. You may be compensated for study-related travel and time. Health insurance is not required. If you qualify, you may receive:
Payment up to $1500, which varies by study.
Conditions:
Cough
Chronic Cough
Asthma
Allergic Asthma
Sinusitis
Featured Trial
Healthy Volunteer Trials
Recruiting
Healthy trials near you are looking for participants to help push medical research forward. Click through to learn more!
Conditions:
Healthy
Featured Trial
Healthy Volunteer Clinical Studies
Recruiting
Find a study looking for volunteers at a study site near you! Some trials offer compensation for time and travel. Click through to learn more about study opportunities.
Conditions:
Healthy
Healthy Volunteers
Featured Trial
High blood pressure (Hypertension) Trials
Recruiting
High blood pressure (Hypertension) trials near you are looking for participants to help push medical research forward. Click through to learn more!
Conditions:
High blood pressure (Hypertension)
Featured Trial
Cardiovascular Disease Trials
Recruiting
Cardiovascular Disease trials near you are looking for participants to help push medical research forward. Click through to learn more!
Conditions:
Cardiovascular Disease
Reversal of Botulinum Neurotoxin Injection Related Dysphonia With Pyridostigmine
Recruiting
The purpose of this study is to evaluate the effects of pyridostigmine (Mestinon) on patient vocal outcomes after undergoing laryngeal botulinum neurotoxin (BoNT) injections, which is a standard treatment for spasmodic dysphonia. Pyridostigmine (Mestinon) has been used for treatment of BoNT overdose, and it is our hope that it will be beneficial in the management of post BoNT breathy phase.
Gender:
All
Ages:
Between 21 years and 100 years
Trial Updated:
07/25/2022
Locations: Eastern Virginia Medical School Ear, Nose, and Throat Surgeons, Norfolk, Virginia
Conditions: Dysphonia, Spastic, Dysphonia, Laryngeal Dystonia
Dipraglurant (ADX48621) for the Treatment of Patients With Parkinson's Disease Receiving Levodopa-based Therapy
Recruiting
This study is designed to evaluate the safety and efficacy of dipraglurant in PD patients with dyskinesia (randomized 1:1 to receive active or placebo) for 12 weeks (1 week at 150 mg per day and 11 weeks at 300 mg per day). The primary efficacy assessment will be based on the Unified Dyskinesia Rating Scale (UDysRS). Patients who complete the 12-week blinded treatment period may have the option to roll into an open-label safety extension study for an additional 12-month treatment period.
Gender:
All
Ages:
Between 30 years and 85 years
Trial Updated:
05/18/2022
Locations: Meridian Clinical Research (Norfolk, Virginia), Norfolk, Virginia
Conditions: Parkinson Disease, Dyskinesia, Drug-Induced, Dyskinesias
Effect of CPAP on Fetal pH at Scheduled C-section in Morbidly Obese Women
Recruiting
The objective of our study is to evaluate the effect of CPAP on umbilical cord acid base status in morbidly obese women at the time of scheduled cesarean delivery. We hypothesize that neonates born to mothers wearing CPAP during the cesarean section will have a higher umbilical artery pH.
Gender:
Female
Ages:
Between 18 years and 45 years
Trial Updated:
04/07/2022
Locations: Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, Eastern Virginia Medical School, Norfolk, Virginia
Conditions: Morbid Obesity, Cesarean Delivery Affecting Fetus
Study to Evaluate the Pharmacodynamics and Efficacy of Leuprolide Tablets (OvarestĀ®) in Women With Endometriosis
Recruiting
The pharmacodynamic endpoint of percentage of subjects with suppressed estradiol level (less than 20 pg/mL) on cycle day 29 is the primary endpoint of the study.
Gender:
Female
Ages:
Between 18 years and 49 years
Trial Updated:
03/21/2022
Locations: Tidewater Clinical Research, Norfolk, Virginia
Conditions: Endometriosis
Laryngeal Nerve Block for Chronic Cough
Recruiting
The purpose of this study is to study the potential benefit of treating chronic neurogenic cough by blocking the nerve responsible for the disease with an injection of local anesthetic/steroid mixture versus a placebo.
Gender:
All
Ages:
18 years and above
Trial Updated:
03/14/2022
Locations: Eastern Virginia Medical School Ear, Nose, and Throat Surgeons, Norfolk, Virginia
Conditions: Laryngeal Nerve Block, Chronic Neurogenic Cough, Laryngeal Hypersensitivity
Home OCT Fluid Visualization Agreement Study
Recruiting
This is a single arm study of home monitoring with the NVHO for 5 weeks with office visits at enrollment, Week 1 and Week 5 (Exit Visit) and, when applicable, Interim Visit(s) triggered by ongoing review by the Reading Center. The study will enroll subjects diagnosed with NV-AMD in at least one eye with attention to the proportion of eyes with IRF and/or SRF. The enrolled eligible subjects will be instructed to self-image the study eye(s) once daily for 5 weeks using a NVHO device at home with s... Read More
Gender:
All
Ages:
55 years and above
Trial Updated:
03/08/2022
Locations: Wagner Macula & Retina Center, Norfolk, Virginia
Conditions: Neovascular Age-related Macular Degeneration
Aspirin for the Prevention of Preeclampsia in Women With Stage 1 Hypertension
Recruiting
In 2017, the American College of Cardiology and the American Heart Association changed the diagnostic criteria for hypertension in non-pregnant adults. The parameters for the diagnosis of stage 1 hypertension were revised from a systolic blood pressure (BP) of 140 to 130 mm Hg and a diastolic BP of 90 to 80 mm Hg. Based on new criteria, stage 1 hypertension is associated with a 2-3 fold increased risk of preeclampsia. There are no data regarding prevention of preeclampsia in women with stage 1 h... Read More
Gender:
Female
Ages:
Between 18 years and 50 years
Trial Updated:
06/25/2021
Locations: Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, Eastern Virginia Medical School, Norfolk, Virginia
Conditions: Pre-Eclampsia
Multi-Center Study to Evaluate the Efficacy and Safety of Sildenafil Cream (3.6%) in Premenopausal Patients With Female Sexual Arousal Disorder
Recruiting
This study is looking to minimize side effects, while maintaining and potentially improving the therapeutic benefit to patients suffering from Female Sexual Arousal Disorder by providing a topical preparation of Sildenafil locally to the vulvar-vaginal tissue.
Gender:
Female
Ages:
21 years and above
Trial Updated:
06/24/2021
Locations: Tidewater Clinical Research, Norfolk, Virginia
Conditions: Female Sexual Arousal Disorder
Self-Reports of Executive Functions in Persons With Parkinson's Disease and Their Significant Others
Recruiting
The investigators are conducting a study to compare the self-reports of executive functions (that is to say, what role cognitive processes such as working memory and attention) in persons with Parkinson's Disease to the reports of executive functions completed by their significant others.
To conduct this study, the investigators need the participation of persons who are diagnosed with Parkinson's Disease and their significant others.
Gender:
All
Ages:
Between 30 years and 79 years
Trial Updated:
06/15/2021
Locations: Old Dominion University, Norfolk, Virginia
Conditions: Parkinsonism or Parkinson's Disease Nos
Microfluidic-based Tactile Sensor in Cardiac Rehabilitation
Recruiting
This study will examine the impact of cardiac rehabilitation on blood vessel health using a newly developed microfluidic-based tactile sensor to assess blood vessel health. The participants will have their blood vessel health measured using a sensor that is placed on top of the skin over the artery before and after exercise (1, 3, 5, 10, 30 and 60 mins). The investigators will study these responses at the first session of cardiac rehabilitation and following 1 and 4 weeks of cardiac rehabilitati... Read More
Gender:
All
Ages:
Between 45 years and 70 years
Trial Updated:
03/19/2021
Locations: Sentara Heart Hospital, Norfolk, Virginia
Conditions: Cardiovascular Diseases, Vascular Stiffness, Endothelial Dysfunction
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