Trials / Completed
CompletedNCT02073734
Effects of Preoperative Dexamethasone Study on QOL After Vaginal Reconstructive Surgery for POP
Effects of Preoperative Dexamethasone on Postoperative Quality of Recovery Following Vaginal Reconstructive Surgery: A Randomized Controlled Trial
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 63 (actual)
- Sponsor
- TriHealth Inc. · Academic / Other
- Sex
- Female
- Age
- 18 Years – 81 Years
- Healthy volunteers
- Not accepted
Summary
The investigators hypothesize that preoperative administration of 8 mg IV dexamethasone will benefit patients' perceived quality of recovery after surgery.
Detailed description
This is a randomized controlled trial involving single administration of 8 mg Dexamethasone per IV preoperatively among women undergoing vaginal reconstructive surgery for pelvic organ prolapse.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Dexamethasone | Dexamethasone 8mg/IV |
| DRUG | Placebo | Placebo given IV |
Timeline
- Start date
- 2013-02-01
- Primary completion
- 2014-08-01
- Completion
- 2014-08-01
- First posted
- 2014-02-27
- Last updated
- 2016-04-21
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT02073734. Inclusion in this directory is not an endorsement.