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Contraception clinical trials

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NCT ID: NCT04425577 Completed - Contraception Clinical Trials

Ultrasound Evaluation Versus Direct Measurement of Uterine Cavity Length

Start date: January 6, 2020
Phase: N/A
Study type: Interventional

To determine if uterine cavity length on transabdominal pelvic ultrasound corresponds to uterine cavity length at time of IUD insertion. If transabdominal pelvic ultrasound is validated as a tool for measuring uterine cavity length, it can be used to guide physicians and subsequently patients in IUD insertion planning.

NCT ID: NCT04423068 Completed - Pregnancy Clinical Trials

Inpatient Adolescent Contraception

Start date: December 10, 2020
Phase: Early Phase 1
Study type: Interventional

The overall goal of this study is to refine and pilot test the investigators novel intervention to offer contraception counseling and initiation for hospitalized female adolescents, focusing on long acting reversible contraception (LARC).

NCT ID: NCT04423055 Completed - Contraception Clinical Trials

Nexplanon Use in Women Primarily Choosing a Combined Oral Contraceptive

NextOC2
Start date: August 13, 2020
Phase: Phase 4
Study type: Interventional

Women currently using or starting a combined oral contraceptive (COC) will be offered study enrollment. Study subjects will have a Nexplanon placed and followed for approximately 12 months to evaluate if they continue the implant, the COC, or both, and to assess bleeding patterns and adverse events.

NCT ID: NCT04396730 Completed - Contraception Clinical Trials

Cannabidiol and Oral Contraceptive Pills: Exploring a Drug-Drug Interaction

Start date: April 8, 2020
Phase: Phase 4
Study type: Interventional

The purpose of this study is to assess how Cannabidiol (CBD) impacts the effectiveness of oral contraceptive (birth control) pills and if CBD changes the possible side effects of birth control pills when CBD and birth control pills are taken at the same time. This study explores the potential interaction between CBD and birth control pills by assessing serum levels of the contraceptive steroid hormones ethinyl estradiol and levonorgestrel in birth control pill users when they also use CBD.

NCT ID: NCT04396483 Recruiting - Contraception Clinical Trials

Dysfunctional Uterine Bleeding After Tubal Sterilization

Start date: June 1, 2021
Phase: N/A
Study type: Interventional

In this study, the investigators will compare the frequency and amount of bleeding after tubal sterilization and salpingectomy

NCT ID: NCT04379102 Completed - Pain Clinical Trials

The Role Of Local Anesthetics in the Management of Adverse Effects Associated With Intrauterine Device Application

Start date: January 20, 2018
Phase:
Study type: Observational

Patients who visited our family planning clinic and opted for IUD application for contraception purposes were also offered NT/TLA treatments simultaneously. 40 patients who matched the inclusion criteria and received IUDs and NT/TLA treatments were included in the study group and 41 patients who only received IUDs were included in the control group. All patients received copper IUDs and none of them were on additional hormonal treatment. Before the insertion of IUD, women in the therapy group received NT treatment with 6ml of 1% procaine injected transvaginal into the cervix at 5 and 7 o'clock localizations. Following IUD insertion, another 6ml of 1% procaine was injected into the Frankenhauser ganglia bilaterally. A final dose of 8ml of 1% procaine was injected into the abdominal trigger points and intracutaneously into the L4-S4 dermatomes as quaddles.

NCT ID: NCT04355598 Not yet recruiting - Contraception Clinical Trials

Cervical Lidocaine-Prilocaine Cream vs Glyceryl Trinitrate Cream in Nulliparous Women With LNG-IUD Insertion

Start date: April 30, 2020
Phase: Phase 4
Study type: Interventional

the aim of the present study is to compare safety and efficacy of cervical Lidocaine-Prilocaine cream versus glyceryl trinitrate cream on pain perception during levonorgestrel- intrauterine device insertion among nulliparous women: a randomized double-blind controlled trial

NCT ID: NCT04340778 Not yet recruiting - Contraception Clinical Trials

Comparative Safety and Efficacy of Vaginal Dinoprostone Versus Lidocaine-prilocaine Cream in Copper IUD Insertion

Start date: April 30, 2020
Phase: Phase 3
Study type: Interventional

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

NCT ID: NCT04339361 Not yet recruiting - Contraception Clinical Trials

Comparative Efficacy of Lidocaine Spray Versus Vaginal Dinoprostone in IUD Insertion

Start date: April 25, 2020
Phase: Phase 4
Study type: Interventional

the aim of this study is to compare the safety and Efficacy of Lidocaine Spray Versus Vaginal dinoprostone in relieving pain during levonorgestrel IUD Insertion in nulliparous women

NCT ID: NCT04339348 Completed - Contraception Clinical Trials

Comparative Safety and Efficacy of Vaginal Misoprostol Versus Lidocaine-prilocaine Cream in Levonorgestrel IUD Insertion

Start date: April 30, 2020
Phase: Phase 3
Study type: Interventional

the aim of the present study is to compare the safety and Efficacy of vaginal misoprostol versus Lidocaine-prilocaine cream in reducing pain during levonorgestrel IUD Insertion in women delivered only by cesarean deliveries