Clinical trials: Contraception
Contraception
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
The purpose of the study is to evaluate the efficacy and safety of a low dose transdermal contraceptive delivery system containing ethinyl estradiol and levonorgestrel.
- Trial name
- NCT01181479
- Testing
- AG200-15 (cycles 1-13), Lessina crossover to AG200-15
- Where
- 80 sites in United States
- Volunteers
- 1,504 people, healthy volunteers welcome
- Sponsor
- Agile Therapeutics
Pregnancy in Adolescence, Counseling
Reducing Adolescent Pregnancy
This multi-site study is employing a brief contraception counseling intervention in the Emergency Department (ED) to shed light on factors that affect decision making as well as barriers and facilitators to conception initiation…
- Conditions
- Pregnancy in Adolescence, Counseling, Contraception Behavior
- Trial name
- NCT04120376
- Testing
- Contraception Counseling
- Where
- 2 sites in United States
- Volunteers
- 144 people, healthy volunteers welcome
- Sponsor
- Children's Hospital of Philadelphia
Contraceptive Usage, Contraception Behavior
Effectiveness Testing of a Videogame Intervention (No Baby No) to Decrease Contraception Non-use Among Adolescents.
The purpose of this study is to evaluate the effectiveness of a videogame compared to an attention/time control at reducing contraceptive non-use among adolescents.
- Trial name
- NCT06990724
- Testing
- Videogame Intervention, Commercial game control
- Where
- 7 sites in United States
- Volunteers
- 850 people, healthy volunteers welcome
- Sponsor
- Weill Medical College of Cornell University
Contraceptive Usage
Increase First-time Mothers' Use of Postpartum Family Planning in Tanzania: The Connect Project
While a growing body of programs have shown promise to increase use of contraception among first time mothers (FTMs), difficulties remain in scaling beyond small pilot areas and institutionalizing within existing systems.
- Trial name
- Connect TZ (NCT06261970)
- Testing
- Connect
- Where
- 2 sites in Tanzania
- Volunteers
- 1,134 people, healthy volunteers welcome
- Sponsor
- George Washington University
Contraception
Assessing Adolescent Use of Nexplanon Over Time
The purpose of this study is to compare Nexplanon decision-making, uptake, satisfaction and contraceptive outcomes (continuation, switching, discontinuation) over a 12-month period among adolescents ages 15-18 to adolescents ages…
- Trial name
- NCT04889079
- Testing
- Contraceptive use (continuation/switching/discontinuation)
- Where
- United States
- Volunteers
- 255 people, healthy volunteers welcome
- Sponsor
- University of Utah
Arterial Thromboembolism, Venous Thromboembolism
Long-term Active Surveillance Study for Oral Contraceptives (LASS)
The objective of this study is to characterize and compare the risks of long-term use of oral contraceptives containing drospirenone and of other established oral contraceptives.
- Conditions
- Arterial Thromboembolism, Venous Thromboembolism, Breast Cancer
- Trial name
- NCT00676065
- Where
- Germany
- Volunteers
- 58,303 people, healthy volunteers welcome
- Sponsor
- Center for Epidemiology and Health Research, Germany
Teen Pregnancy
Evaluation of a Need to Know (N2K): A New Sex Education Program for High School Students
This trial evaluated the impact of N2K, a three-year quasi-experimental study to delay sexual initiation and increase condom and contraception use among high school students.
- Trial name
- N2K (NCT02539602)
- Testing
- The Need to Know students received the N2K curriculum as described previously
- Volunteers
- 1,616 people, healthy volunteers welcome
- Sponsor
- The University of Texas Health Science Center at San Antonio
Postpartum
Home-based Delivery of the Contraceptive Implant in Postpartum Guatemalan Women
Abstract Background: Postpartum contraception is important to prevent unintended and closely spaced pregnancies following childbirth.
- Trial name
- NCT04005391
- Testing
- Offer of Participant's Choice of Contraception Method
- Where
- 2 sites in United States, Guatemala
- Volunteers
- 208 people, healthy volunteers welcome
- Sponsor
- University of Colorado, Denver
HIV Infections, Contraception
PrEParing Family Planning Clinics to Streamline Integration of HIV Prevention Services for Young Women in Kenya
This a prospective, open-label implementation project to catalyze integration of HIV prevention and PrEP care services for adolescent girls and young women in family planning clinics in Kenya.
- Conditions
- HIV Infections, Contraception, STI
- Trial name
- NCT04666792
- Testing
- PrEP
- Where
- Kenya
- Volunteers
- 25,457 people, healthy volunteers welcome
- Sponsor
- University of Washington
Unintended Pregnancy, Family Planning
Addressing Reproductive Coercion in HEalth Settings - Kenya
The primary purpose of this research is to conduct a small matched cluster control trial of an intervention designed to address reproductive coercion and unintended pregnancy (ARCHES - Addressing Reproductive Coercion within…
- Conditions
- Unintended Pregnancy, Family Planning, Intimate Partner Violence (IPV)
- Trial name
- ARCHES (NCT03534401)
- Testing
- ARCHES Kenya
- Where
- United States
- Volunteers
- 659 people, healthy volunteers welcome
- Sponsor
- University of California, San Diego
Pain
Study of Pain Control With Hormonal IUS Insertion
This study aims to compare pain during insertion of the Skyla® IUS using a 100mm visual analog scale (VAS) among 92 young women aged 14 to 22 years randomized to receive a paracervical (n=46) block versus a sham paracervical…
- Trial name
- SOPHI (NCT02352714)
- Testing
- Paracervical Nerve Block
- Where
- 3 sites in United States
- Volunteers
- 98 people, healthy volunteers welcome
- Sponsor
- Children's Hospital of Philadelphia
Contraception
Transatlantic Active Surveillance on Cardiovascular Safety of NuvaRing (TASC)
The objective of this study is to characterize and compare the risks of short- and long-term use of NuvaRing® with marketed combined oral contraceptives.
- Trial name
- TASC (NCT00524771)
- Where
- Germany
- Volunteers
- 34,100 people, healthy volunteers welcome
- Sponsor
- Center for Epidemiology and Health Research, Germany
Reproductive Health
Study on Mhealth and Reproductive Health in Teens
The purpose of the Study on Mhealth and Reproductive Health in Teens (SMART) is to evaluate the effectiveness of using text messages to improve the knowledge, communication, and attitudes about reproductive health among female…
- Trial name
- SMART (NCT02031575)
- Testing
- Interactive Treatment, Basic Treatment, Control, comparator arm
- Where
- Ghana
- Volunteers
- 1,419 people, healthy volunteers welcome
- Sponsor
- Harvard University
Unintended Pregnancy, Family Planning
Jovenes Sanos: Preventing IPV and RC
The primary purpose of this research is to conduct a small matched cluster control trial of an intervention designed to address reproductive coercion and unintended pregnancy (ARCHES - Addressing Reproductive Coercion within…
- Conditions
- Unintended Pregnancy, Family Planning, Intimate Partner Violence (IPV)
- Trial name
- NCT03660514
- Testing
- Jovenes Sanos
- Where
- 3 sites in United States, Mexico
- Volunteers
- 124 people, healthy volunteers welcome
- Sponsor
- University of California, San Diego
Contraception
RCT: Can a Single Counseling Phone Call Improve Contraception After an Abortion?
Hypothesis: Use of an effective contraceptive six weeks after abortion will be higher in the treatment group than in the control group.
- Trial name
- PPR (NCT01199952)
- Testing
- Treatment group: receives counseling phone call intervention
- Where
- United States
- Volunteers
- 207 people, healthy volunteers welcome
- Sponsor
- University of California, San Francisco
Healthy
Pericoital Oral Contraception With Levonorgestrel
A prospective, open-label, single arm, multicenter study to evaluate efficacy, safety and acceptability of pericoital oral contraception with levonorgestrel
- Trial name
- NCT00922233
- Testing
- levonorgestrel
- Where
- 4 sites in United States, Brazil
- Volunteers
- 72 people, healthy volunteers welcome
- Sponsor
- FHI 360
Contraception
Comparative Safety and Efficacy of Vaginal Dinoprostone Versus Lidocaine-prilocaine Cream in Copper IUD Insertion
the aim of the present study is to Compare Safety and Efficacy of Vaginal dinoprostone Versus Lidocaine-prilocaine Cream in copper IUD Insertion in nulliparous women: a randomized controlled trial
- Trial name
- NCT04340778
- Testing
- vaginal dinoprostone, Lidocaine-prilocaine Cream
- Volunteers
- 210 people, healthy volunteers welcome
- Sponsor
- Cairo University
Peer Counseling, LARC Desire
Influence of Peer Mentoring on Adolescent Contraceptive Decision Making
This is a prospective, randomized-controlled trial in which subjects will be randomized to receive either routine contraceptive counseling or peer mentoring plus routine contraceptive counseling.
- Trial name
- ImPACCT (NCT02157285)
- Testing
- Peer Mentor Counseling
- Where
- United States
- Volunteers
- 110 people, healthy volunteers welcome
- Sponsor
- University of Pennsylvania
Postpartum Contraception, Family Planning
Labor and Delivery Implant Insertion: A Randomized Controlled Trial
A barrier to initiating progestin contraceptives in the early postpartum period is the concern of interference with breastfeeding, specifically lactogenesis.
- Trial name
- LADII (NCT02866643)
- Testing
- Etonogestrel-Immediate, Etonogestrel-Delayed
- Where
- United States
- Volunteers
- 95 people, healthy volunteers welcome
- Sponsor
- Stanford University
Safety
Safety, Compliance and Pharmacokinetics of Estetrol Monohydrate/Drospirenone 15/3 mg in Post-menarchal Female Adolescents
To evaluate the safety, compliance, and pharmacokinetics profile of estetrol monohydrate (E4) 15 mg combined with drospirenone (DRSP) 3 mg in post-menarchal participants between the age of 12 and 17 years + 2 months.
- Trial name
- NCT04792385
- Testing
- E4/DRSP 15/3 mg combined tablet
- Where
- 23 sites in Estonia, Finland and 4 more
- Volunteers
- 145 people, healthy volunteers welcome
- Sponsor
- Estetra