Trials / Unknown
UnknownNCT00209872
Optimal Multimodal Analgesia in Abdominal Hysterectomy
- Status
- Unknown
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 60 (estimated)
- Sponsor
- Hvidovre University Hospital · Academic / Other
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to test the current standard of care (SOC) treatment for abdominal hysterectomy with a group receiving SOC minus epidural analgesia plus additional perioperative analgesics in terms of postoperative abilities, postoperative nausea and vomiting (PONV), pain and discharge time from the PACU (post-anaesthesia care unit).
Detailed description
Aim of the study: to compare postoperative complaints (PONV, pain, etc) and PACU discharge time between two groups, for patients admitted for planned abdominal hysterectomy with or without BSO: * A: standard of care (SOC) receiving paracetamol, celecoxib, epidural analgesia, dexamethasone, ondansetron and droperidol, and general anaesthesia with propofol, remifentanil and cisatracurium * B: SOC with sham epidural analgesia, preoperative gabapentin, intraoperative lidocaine, s-ketamine and sufentanil
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Gabapentin | |
| DRUG | Lidocaine | |
| DRUG | S-ketamine | |
| PROCEDURE | Epidural analgesia |
Timeline
- Start date
- 2005-10-01
- First posted
- 2005-09-21
- Last updated
- 2007-11-07
Locations
1 site across 1 country: Denmark
Source: ClinicalTrials.gov record NCT00209872. Inclusion in this directory is not an endorsement.