Clinical Trials Directory

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

TypeNameDescription
DRUGGabapentin
DRUGLidocaine
DRUGS-ketamine
PROCEDUREEpidural 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.