Trials / Completed
CompletedNCT01106547
The Effect of a Preoperative Single-dose Methylprednisolone on the Postoperative Rehabilitation After Abdominal Hysterectomy
The Effect of a Preoperative Single-dose Methylprednisolone on the Postoperative Rehabilitation After Abdominal Hysterectomy: A Prospective, Double Blinded, Placebo Controlled Study
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 55 (estimated)
- Sponsor
- Holbaek Sygehus · Academic / Other
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to evaluate the effect of 125 mg methylprednisolone, given intravenously 60-90 minutes before abdominal surgery,on the postoperative rehabilitation after abdominal hysterectomy.Sodium Chloride is the placebo. The following parameters are registered: 1. Pain 3, 6 and 24 hours postoperatively and 2-7 days after surgery. 2. The postoperative use of additional analgesics. 3. Inflammatory parameters before and after surgery. 4. Time until mobilization. 5. Time until discharge.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Methylprednisolone 125mg | Single dose 60-90 minutes preoperatively |
| DRUG | Sodium Chloride 2 ml | Single dose 60-90 min preoperatively |
Timeline
- Start date
- 2009-08-01
- Primary completion
- 2011-09-01
- Completion
- 2011-10-01
- First posted
- 2010-04-20
- Last updated
- 2011-10-13
Locations
1 site across 1 country: Denmark
Source: ClinicalTrials.gov record NCT01106547. Inclusion in this directory is not an endorsement.