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Optimal Multimodal Analgesia in Abdominal Hysterectomy

NCT00209872 · Status: UNKNOWN · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2007-11-07

No results posted yet for this study

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).

Conditions

  • Planned Abdominal Hysterectomy

Interventions

DRUG

Gabapentin

DRUG

Lidocaine

DRUG

S-ketamine

PROCEDURE

Epidural analgesia

Sponsors & Collaborators

  • Hvidovre University Hospital

    lead OTHER

Principal Investigators

  • Kenneth Jensen, M.D. · Dept. of Anaesthesia, Acute Pain Service, Hvidovre Hospital, Copenhagen, Denmark

  • Claus Lund, Dr. Med. Sci. · Dept. of Anaesthesia, Hvidovre Hospital, Copenhagen, Denmark

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-10-31

Countries

  • Denmark

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00209872 on ClinicalTrials.gov