Viewing Study NCT00209872



Ignite Creation Date: 2024-05-05 @ 11:59 AM
Last Modification Date: 2024-10-26 @ 9:18 AM
Study NCT ID: NCT00209872
Status: UNKNOWN
Last Update Posted: 2007-11-07
First Post: 2005-09-14

Brief Title: Optimal Multimodal Analgesia in Abdominal Hysterectomy
Sponsor: Hvidovre University Hospital
Organization: Hvidovre University Hospital

Study Overview

Official Title: None
Status: UNKNOWN
Status Verified Date: 2005-09
Last Known Status: NOT_YET_RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief 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

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
eudraCT 2005-003595-38 None None None