Surgical Treatments Outcomes Project for Dysfunctional Uterine Bleeding (STOP-DUB)
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT00114088|
Recruitment Status : Completed
First Posted : June 14, 2005
Last Update Posted : June 24, 2005
|Condition or disease||Intervention/treatment||Phase|
|Menorrhagia Uterine Bleeding||Procedure: hysterectomy Procedure: endometrial ablation||Phase 3|
|Study Type :||Interventional (Clinical Trial)|
|Enrollment :||242 participants|
|Intervention Model:||Parallel Assignment|
|Official Title:||Surgical Treatments Outcomes Project for Dysfunctional Uterine Bleeding (STOP-DUB)|
|Study Start Date :||November 1997|
|Study Completion Date :||January 2004|
- Randomized trial: Impact of surgery on bleeding, pain,
- fatigue, and major problem (symptom) leading the woman to seek treatment for her condition.
- Observational study: changes over time in treatment selected, DUB-related symptoms, and quality of life.
- Randomized trial: Impact of surgery on primary outcomes at time points after 1 year, quality of life, activity limitation, sexual functioning, urinary incontinence, surgical complications, additional surgery, resource utilization.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00114088
|Principal Investigator:||Kay Dickersin, PhD||Brown University|