Sayana Press UK Self-Injection Study
NCT03034057 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 169
Last updated 2019-10-18
Summary
A one-year evaluation of Sayana Press self injection in women of reproductive age in the United Kingdom (UK).
Conditions
- Contraception
Interventions
- DRUG
-
Sayana Press
Sayana Press in the Uniject injection system
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Pfizer CT.gov Call Center · Pfizer
Study Design
- Purpose
- PREVENTION
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 45 Years
- Sex
- FEMALE
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2017-08-23
- Primary Completion
- 2018-12-07
- Completion
- 2018-12-07
Countries
- United Kingdom
Study Locations
More Related Trials
-
Clinical Study of Depo Provera Comparing Lay Health Workers and Clinically-trained Health Workers
NCT03255941 ·Status: COMPLETED ·Phase: EARLY_PHASE1
-
Efficacy and Safety Oral Contraceptive Study
NCT00185484 ·Status: COMPLETED ·Phase: PHASE3
-
Self Administration of Subcutaneous Depot Medroxyprogesterone Acetate
NCT00770887 ·Status: COMPLETED
-
Open-Label Study to Evaluate the Safety and Efficacy of a Low-Dose 28-Day Oral Contraceptive
NCT00362479 ·Status: COMPLETED ·Phase: PHASE3
-
Study to Investigate Compliance With the Oral Contraceptive SH T00186D in a Flexible Extended Regimen Supported by a Dispenser With a Reminder Function
NCT01257984 ·Status: COMPLETED ·Phase: PHASE3
-
An Open-label Study to Evaluate Contraceptive Efficacy and Safety of the Transdermal Contraceptive System of Norelgestromine and Ethinyl Estradiol
NCT00307632 ·Status: COMPLETED ·Phase: PHASE4
-
Depo Provera Self-Administration Study: Putting a Patient-Centered Practice to the Test at Planned Parenthood
NCT02509767 ·Status: COMPLETED ·Phase: PHASE4
-
Study of Safety and Efficacy of an Oral Contraceptive
NCT00391807 ·Status: COMPLETED ·Phase: PHASE3
-
AMP002 Phase III Contraceptive Study
NCT03243305 ·Status: COMPLETED ·Phase: PHASE3
-
A Multicenter Study to Evaluate the Safety of Seasonique, an Oral Contraceptive.
NCT00196352 ·Status: COMPLETED ·Phase: PHASE3
-
A Comparing Study Between SJ04 and Ovidrel® in Healthy Subjects
NCT06599528 ·Status: RECRUITING ·Phase: PHASE1
-
Efficacy and Safety of Two Flexible Extended Regimens of BAY86-5300 (SH T00186D) in Comparison With the Conventional Regimen of YAZ
NCT00567164 ·Status: COMPLETED ·Phase: PHASE3
-
Open-label Study to Evaluate the Efficacy and Safety of an Extended-cycle, Low Dose Combination Oral Contraceptive
NCT00196326 ·Status: COMPLETED ·Phase: PHASE3
-
Lower Dose Depo Provera® Contraceptive Injection
NCT02732418 ·Status: COMPLETED ·Phase: PHASE1
-
A Study of Oral Contraception Under Simulated OTC Conditions
NCT03559010 ·Status: TERMINATED ·Phase: PHASE3
-
Study Evaluating Levonorgestrel and Ethinyl Estradiol for Oral Contraception
NCT00245921 ·Status: COMPLETED ·Phase: PHASE3
-
A Study to Determine the Effects of PF-04965842 on the Pharmacokinetics of Oral Contraceptive Steroids in Healthy Female Subjects
NCT03662516 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Evaluate the Efficacy and Safety of Subcutaneous Levonorgestrel Butanoate for Female Contraception
NCT07222228 ·Status: NOT_YET_RECRUITING ·Phase: PHASE2
-
The Safety and Effectiveness of the Essure (Model ESS505) Device to Prevent Pregnancy in Women
NCT01861886 ·Status: COMPLETED ·Phase: NA
-
YAZ Post Authorization Safety Study (PASS)/Post Authorization Efficacy Study (PAES) in China
NCT02710708 ·Status: COMPLETED ·Phase: PHASE4
-
Impact of ESSURE Devices Withdrawal on the Symptomatology of Patients
NCT03623126 ·Status: COMPLETED
-
A Study of Remternetug (LY3372993) in Healthy Participants
NCT07056309 ·Status: COMPLETED ·Phase: PHASE1
-
A Multicenter, Non-Comparative Trial on the Contraceptive Efficacy, Safety, and Tolerability of LPRI-424, 13 Cycles
NCT03945513 ·Status: COMPLETED ·Phase: PHASE3
-
YAZ, Oral Contraceptive Registration in China
NCT00819312 ·Status: COMPLETED ·Phase: PHASE3
-
Specific Supplementation in Counteracting the Adverse Effects of Oral Contraceptives
NCT07071389 ·Status: WITHDRAWN ·Phase: NA