Now Available: Final Rule for FDAAA 801 and NIH Policy on Clinical Trial Reporting
519 studies found for:    contraception AND (woman OR women OR female) NOT (male OR men)
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Rank Status Study
1 Completed Safety, Tolerability, and Efficacy of ellaOne® (Ulipristal Acetate) for Emergency Contraception in Postmenarcheal Adolescent Girls and Women
Condition: Contraception
Intervention: Drug: ellaOne® (ulipristal acetate)
2 Unknown  Increasing Contraception Utilization Among Women Prescribed Teratogenic Medications
Condition: Teratogenesis
Intervention: Behavioral: Education
3 Completed Emergency Contraception and Body Weight: Pilot Study
Conditions: Contraception;   Body Weight
Intervention: Drug: Levonorgestrel (LNG)-based Emergency Contraception
4 Unknown  The Effect of Hormonal Contraception on Female
Condition: Adverse Effect of Oral Contraceptives, Initial Encounter
Interventions: Other: Contraceptives, Oral, Combined;   Other: Controls
5 Active, not recruiting Video Counseling for Effective Postpartum Contraception
Condition: Contraception
Intervention: Behavioral: LARC First Video
6 Not yet recruiting An Intervention Delivered by Text Message to Increase the Acceptability of Effective Contraception Among Young Women in Palestine
Condition: Contraception
Interventions: Behavioral: Contraceptive text messages;   Other: Text messages not about contraception
7 Completed Evaluation of Women's Experience With EVRA (Norelgestromin + Ethinyl Estradiol) Transdermal Contraceptive Patch Compared With Previous Methods of Contraception.
Conditions: Contraception;   Female Contraception
Intervention: Drug: norelgestromin + ethinyl estradiol
8 Completed The Effect of Uterine Size and Posture on Intrauterine Contraception in Nulliparous Women
Condition: Intrauterine Contraception.
Intervention: Other: Evaluation of uterine size and posture with ultrasound, IUD insertion, one year follow-up.
9 Completed A Randomized Trial of IUD Versus Hormonal Contraception in HIV-infected Women in Zambia
Conditions: Pregnancy;   HIV Infection
Interventions: Device: Copper T Intrauterine Contraceptive Device;   Drug: Hormonal Contraception
10 Active, not recruiting Integration of Family Planning Services Into Anticoagulation Monitoring Services
Condition: Contraception
Intervention: Other: Integrated Family Planning Services
11 Unknown  Egyptian Women Knowledge and Use of Different Contraceptive Methods
Condition: Contraception
Intervention:
12 Not yet recruiting An Intervention Delivered by App Instant Messaging to Increase Use of Effective Contraception Among Young Women in Bolivia
Condition: Contraception
Interventions: Behavioral: Contraceptive instant messages;   Other: Mobile phone app
13 Completed Use of Motivational Interviewing to Increase Contraception Use Among Young Women
Condition: Unplanned Pregnancy
Intervention: Behavioral: Counseling Intervention
14 Not yet recruiting Evaluation of Vitamin D in Women With PCOS and Sexual Dysfunction
Conditions: Female Sexual Dysfunction;   Polycystic Ovary Syndrome
Interventions: Dietary Supplement: Vitamin D;   Drug: Hormonal contraception
15 Active, not recruiting EC PK in Women With Normal and Obese BMI
Condition: Contraception
Interventions: Drug: Levonorgestrel 1.5mg;   Drug: Ulipristal acetate 30mg
16 Active, not recruiting Evaluation of Safety and Effectiveness of the Essure (Model ESS505) Device to Prevent Pregnancy in Women
Condition: Contraception
Intervention: Device: ESS505 (BAY1454033)
17 Completed Descriptive, Prospective, Non-interventional Study (NIS) to Describe Mirena and Amenorrhea Related Acceptability in Contraception Indication in Medical Practice
Condition: Female Contraception
Intervention: Drug: Levonorgestrel IUD (Mirena, BAY86-5028)
18 Completed Study of the Copper IUD or Oral Levonorgestrel and the Levonorgestrel IUD for Women Seeking Emergency Contraception
Condition: Emergency Contraception
Interventions: Drug: Copper IUD;   Drug: Levonorgestrel IUD
19 Completed The Safety and Effectiveness of the Essure (Model ESS505) Device to Prevent Pregnancy in Women
Condition: Contraception
Intervention: Device: ESS505 (BAY1454033)
20 Terminated
Has Results
Adiana Post-Approval Clinical Study (APACS)
Condition: Women Contraception
Intervention:

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Study has passed its completion date and status has not been verified in more than two years.