Clinical Trials Directory

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

TypeNameDescription
DRUGMethylprednisolone 125mgSingle dose 60-90 minutes preoperatively
DRUGSodium Chloride 2 mlSingle 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.