Trials / Completed
CompletedNCT02819609
Comparing Patient-Centered Outcomes After Treatment for Uterine Fibroids
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 12,234 (actual)
- Sponsor
- Quintiles, Inc. · Industry
- Sex
- Female
- Age
- 18 Years – 54 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this observational, retrospective database study of patients with uterine fibroids is to compare the durability of symptom relief after uterus-conserving treatments for symptomatic fibroids in terms of incidence of, and time to, new or recurrent symptoms and subsequent procedures and evaluate the effect stakeholder participation had on the research process.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | myomectomy | Myomectomy as part of routine clinical care |
| PROCEDURE | endometrial ablation | Endometrial ablation as part of routine clinical care |
| PROCEDURE | uterine artery embolization | Uterine artery embolization as part of routine clinical care |
| PROCEDURE | MRI-guided focused ultrasound ablation | MRI-guided focused ultrasound ablation as part of routine clinical care |
Timeline
- Start date
- 2014-11-01
- Primary completion
- 2015-01-01
- Completion
- 2015-01-01
- First posted
- 2016-06-30
- Last updated
- 2016-06-30
Source: ClinicalTrials.gov record NCT02819609. Inclusion in this directory is not an endorsement.