Clinical Trials Logo
  1. Home
  2. Metrorrhagia
  3. NCT00307801

Efficacy and Safety Study for the Treatment of Dysfunctional Uterine Bleeding

Metrorrhagia Clinical Trial

Official title:
A Multicenter, Double-Blind, Randomized, Parallel-Group, Placebo-Controlled, 7 Cycle Duration (196 Days), Phase 3 Study of Oral Estradiol Valerate/Dienogest Tablets for the Treatment of Dysfunctional Uterine Bleeding.

Clinical Trial Summary

The purpose of this study is to determine whether the study drug is safe and effective in the treatment of dysfunctional uterine bleeding.

Clinical Trial Description

The study has previously been posted by Schering AG, Germany. Schering AG, Germany has been renamed to Bayer HealthCare AG, Germany. Bayer HealthCare AG, Germany is the sponsor of the trial. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00307801
Study type Interventional
Source Bayer
Contact
Status Completed
Phase Phase 3
Start date February 2006
Completion date May 2008
View Details
See also
  Status Clinical Trial Phase
Completed NCT02824224 - Tamoxifen to Reduce Unscheduled Bleeding in New Users of the Levonorgestrel-releasing Intrauterine System (LNG-IUS) Phase 4
Completed NCT00563576 - Pilot Study of Femring Estrogen Supplementation During Depo-Provera Initiation N/A
Completed NCT00152256 - A Study to Evaluate of the Safety and Effectiveness of Asoprisnil in Treating Women With Uterine Fibroids Phase 3
Completed NCT00156195 - Study to Evaluate the Safety of Asoprisnil in the Treatment of Uterine Fibroids Phase 3
Completed NCT00160381 - A Study to Evaluate the Safety and Effectiveness of Asoprisnil in the Treatment of Uterine Fibroids Phase 3
Completed NCT01436513 - A Study To Compare The Amount Of Premarin Components That Is Absorbed Into The Blood Of Japanese Healthy Postmenopausal Women Following Oral Administration Of Two Different Tablets Of Premarin Under Fast and Fed Conditions. Phase 1
Completed NCT00156156 - Study of Asoprisnil in the Treatment of Uterine Fibroids. Phase 3
Completed NCT00344383 - An Open-Label Study Evaluating Breakthrough Bleeding and Spotting With Norgestimate/Ethinyl Estradiol Tablets Administered as an Extended Regimen Phase 2
Recruiting NCT05538689 - Surgical Myomectomy Followed by Oral Myfembree Versus Standard of Care Trial (SOUL) Phase 4
Completed NCT03121560 - Acceptability and Tolerance of Hysteroscopy and Hysterosonography in Consultation N/A
Completed NCT05406960 - Therapeutic Effect of Herbal Infusion on Menometrorrhagia N/A
Completed NCT01918072 - Controlled Trial of Tele-Support and Education for Womens Health Care in CBOCs
Recruiting NCT03230994 - Cooperative Adenomyosis Network
Completed NCT01638923 - Study of a 4-phasic Oral Contraceptive for the Treatment of Heavy Menstrual Bleeding Phase 3
Completed NCT01647360 - Severity of Bleeding as a Predictor of Quality of Life (QoL) in Women With Heavy Menstrual Bleeding (HMB) Under Dydrogesterone Treatment N/A
Completed NCT00152269 - Treatment of Uterine Fibroids With Asoprisnil(J867) Phase 3
Withdrawn NCT01557023 - Clinical Trial With Combination of Dienogest/Ethytnilestradiol and Drosperidona/Ethyniestradiol Phase 3
Completed NCT01865929 - Minimally Invasive Benign Hysterectomy N/A
Completed NCT01793584 - Surgical Success After Laparoscopic vs Abdominal Hysterectomy N/A
Completed NCT02311478 - Tracking IUD Bleeding Experiences: An Evaluation of Bleeding Profiles in New Intrauterine Device Users N/A