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Contraception Clinical Trials
A listing of 20 Contraception clinical trials actively recruiting volunteers for paid trials and research studies in various therapeutic areas.
1 - 12 of 20
There are currently 20 active clinical trials seeking participants for Contraception research studies. The states with the highest number of trials for Contraception participants are California, Florida, Texas and Pennsylvania.
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
Transcranial Magnetic Stimulation (TMS) for Obsessive Compulsive Disorder (OCD)
Recruiting
Transcranial magnetic stimulation (TMS) is an FDA-approved, non-invasive form of brain stimulation for OCD. TMS has been shown to be an effective form of treatment in individuals with OCD. By using a form of TMS termed theta-burst stimulation (TBS), we hope that this will result in a more effective treatment by producing faster symptom reduction. We are trialing a novel form of accelerated TMS, where we will deliver ten 10-minute sessions per day, for 5 days. This study will compare the efficacy of TMS for OCD at two distinct brain regions. Participants will be randomized into one of two study groups, and receive stimulation at either the DMPFC or R-OFC. Both regions have been linked to OCD by research. Patients that don't respond to their study region will have the option to receive stimulation at the other region.
Conditions:
Obsessive-Compulsive Disorder
Obsessive Compulsive Disorder
Obsessive Compulsive Disorder (OCD)
Obsessive-Compulsive Disorder (OCD)
Obsessive-compulsive Disorders and Symptoms
Featured Trial
Type 2 Diabetes Clinical Trial
Recruiting
Can changing your breakfast improve your type 2 diabetes? Join this online study from the University of Michigan.
Conditions:
Type 2 Diabetes
Diabetes Mellitus Type 2 in Obese
Diabetes Type Two
Prospective Multi-Center Trial for FemBloc Permanent Birth Control
Recruiting
Prospective, multi-center, international, unblinded, single-arm trial of subjects undergoing FemBloc followed by ultrasound confirmation test.
Gender:
FEMALE
Ages:
Between 21 years and 50 years
Trial Updated:
01/24/2025
Locations: Stanford University, Palo Alto, California +5 locations
Conditions: Contraception
Contraceptive Efficacy Study of Ovaprene
Recruiting
This will be a multi-center, single arm, open-label study of Ovaprene, a non-hormonal intravaginal ring, to investigate the contraceptive effectiveness, safety and acceptability of Ovaprene.
Gender:
FEMALE
Ages:
Between 18 years and 40 years
Trial Updated:
01/23/2025
Locations: Precision Trials AZ, Phoenix, Arizona +23 locations
Conditions: Contraception
Intervening on Women's Health for Rural Young Cancer Survivors
Recruiting
The purpose of this pilot study is to evaluate the feasibility of a multi-component intervention to improve young female cancer survivors' engagement in goal-concordant reproductive health care. The investigators hypothesize that implementation of the intervention will result in increased young cancer survivors' engagement in goal-concordant reproductive health care.
Gender:
FEMALE
Ages:
Between 15 years and 50 years
Trial Updated:
01/08/2025
Locations: San Diego State University - Imperial Valley/ School of Nursing, Brawley, California +3 locations
Conditions: Cancer, Fertility Issues, Contraception
Contraception Navigator Program
Recruiting
The goal of this study is to pilot test the IN-Control Birth Control Navigator Program in Central Indiana for use by adolescents who would like to access birth control. The investigators hypothesize that facilitating access to contraception through our intervention will ultimately result in increased feelings of autonomy around these decisions and use of hormonal contraception.
Gender:
FEMALE
Ages:
Between 15 years and 19 years
Trial Updated:
12/12/2024
Locations: Indiana University School of Medicine, Indianapolis, Indiana
Conditions: Contraception, Contraceptive Usage, Health Care Utilization
Patient-centered Information on Permanent Contraception
Recruiting
The goal of this study is to understand whether providing information to women with a strong desire to avoid future pregnancy about how tubal sterilization compares to long-acting reversible contraceptives improves perceived access to available contraceptives.
Participants will:
* Complete a baseline survey
* Receive access to web-based educational resources
* Complete a brief follow up survey immediately after exploring these web-based resources
* Complete a follow-up survey 3 months after en... Read More
Gender:
FEMALE
Ages:
Between 21 years and 45 years
Trial Updated:
12/03/2024
Locations: University of California, San Francisco, San Francisco, California
Conditions: Contraception, Reproductive Behavior, Contraception Behavior
Oral Contraceptive Pill (OCP) Pharmacogenomics
Recruiting
The goal of this clinical trial is to evaluate how differences in specific parts of our DNA can influence how individual bodies break down the hormones contained within oral contraceptive pills, which could affect how well these birth control pills work to prevent pregnancy. The investigators are also interested in exploring how these differences in our DNA can also explain why patients taking the exact same formulation of birth control pill will experience very different side effects. The main... Read More
Gender:
FEMALE
Ages:
Between 18 years and 45 years
Trial Updated:
11/13/2024
Locations: University of Colorado Anschutz Medical Campus, Aurora, Colorado +1 locations
Conditions: Contraception, Pharmacogenomic Drug Interaction
The HOP-STEP Intervention: Improving Maternal Health in Women With Lupus sIRB
Recruiting
While the HOP-STEP (Healthy Outcomes in Pregnancy with SLE Through Education of Providers) program has been demonstrated to be effective in improving provider confidence, increasing contraception documentation, and facilitating equitable pregnancy planning care in a single sub-specialty clinic here at Duke, the delivery of HOP-STEP may need to be changed to increase its fit with the local context at the University of Chicago Medical Center (UCMC) and subsequent locations. Thus, the investigators... Read More
Gender:
ALL
Ages:
18 years and above
Trial Updated:
10/11/2024
Locations: University of Chicago Medical Center, Chicago, Illinois
Conditions: Systemic Lupus Erythematosus, Contraception
A 3-way Crossover Clinical Investigation to Assess the Performance of Two Different Sized Polyurethane Condoms Versus a Latex Condom in Healthy Monogamous Couples.
Recruiting
This investigation is designed to evaluate the performance rate of two polyurethane male condoms with different sizes and thicknesses versus a standard natural rubber latex (NRL) male condom.
The purpose of this study is to see how well the experimental condoms perform compared to the latex rubber condom (for example, how often the different condom types break or slip off the penis).
Sponsor also wants to find out how well couples like using the three condom types and whether they experience a... Read More
Gender:
ALL
Ages:
Between 18 years and 60 years
Trial Updated:
08/29/2024
Locations: Essential Access Health-Berkeley, Berkeley, California +2 locations
Conditions: Contraception
Using the Connect: Game Based Intervention
Recruiting
The study aims to implement Using the Connect (UTC), an innovative, game-based intervention designed to increase protective factors and decrease adolescent pregnancies. This intervention will be implemented in Texas middle schools and community-based organizations. The long-term goal is to promote optimal health in youth and prevent adolescent pregnancy in populations disproportionately impacted by adolescent pregnancy and sexually transmitted infection (STI) rates. The short-term objective is t... Read More
Gender:
ALL
Ages:
Between 9 years and 15 years
Trial Updated:
08/20/2024
Locations: HYPE, Bryan, Texas +1 locations
Conditions: Adolescent Behavior, Contraception, Health Behavior
Endometrial Biopsy in Progestin Contraceptive Users
Recruiting
The purpose of the study is to learn more about menstrual changes in progestin contraception users. The investigators are hoping to find out what changes in the endometrium lead to different bleeding patterns during the first year of progestin contraception use. Participants will choose to receive the contraceptive implant (Etonogestrel implant also called Nexplanon) or the contraceptive injectable (Depo-medroxyprogesterone acetate (DMPA) also called Depo-Provera) for up to 12 months. They will... Read More
Gender:
FEMALE
Ages:
Between 18 years and 40 years
Trial Updated:
08/16/2024
Locations: OHSU, Portland, Oregon
Conditions: Contraception
The Over The Counter Pill National Study
Recruiting
This is a prospective cohort study of individuals purchasing the oral contraceptive pill over the counter (OTC) in pharmacies in 32 US states. The comparison group is people receiving a prescription (Rx) for oral contraception. Both groups will be followed for one year to examine contraceptive continuation rates. This study will also identify who is using the pill OTC and why and evaluate differences in pregnancy intention and measures of contraceptive agency between the two groups.
Gender:
FEMALE
Ages:
Between 12 years and 51 years
Trial Updated:
08/16/2024
Locations: Oregon Health & Science University, Portland, Oregon
Conditions: Contraception, Contraception Behavior, Contraceptive Usage, Health Care Utilization
Intravenous Ketorolac Administration to Attenuate Post-procedural Pain Associated With Intrauterine Device Placement
Recruiting
Intrauterine devices (IUDs) are a popular form of long-acting reversible contraception, with a high efficacy rate and few side effects. The insertion procedure for IUDs can be uncomfortable and painful. Sedation may be needed to improve patient comfort. The use of IUDs is increasing in the adolescent population, but perceived pain is a barrier to placement.
Propofol is a commonly used agent for pediatric procedural sedation, but it has no analgesic properties. Ketorolac, a nonsteroidal anti-inf... Read More
Gender:
FEMALE
Ages:
Between 13 years and 21 years
Trial Updated:
07/30/2024
Locations: Arkansas Childrens Hospital, Little Rock, Arkansas
Conditions: IUD, Healthy Female, Contraception, IUD Insertion Complication
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