Viewing Study NCT00149253



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Last Modification Date: 2024-10-26 @ 9:14 AM
Study NCT ID: NCT00149253
Status: COMPLETED
Last Update Posted: 2005-09-08
First Post: 2005-09-06

Brief Title: Pre-Emptive Analgesia Efficacy of Etoricoxib for Postoperative Pain
Sponsor: Khon Kaen University
Organization: Khon Kaen University

Study Overview

Official Title: A Randomized Double-Blind Controlled Trial of Etoricoxib as a Pre-Emptive Analgesic for Abdominal Hysterectomy
Status: COMPLETED
Status Verified Date: 2004-10
Last Known Status: None
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: Taken together studies of the value of pre-emptive analgesia are inconclusive This randomized double-blind dose-ranging placebo-controlled study was therefore designed to test that a reduction in post-operative morphine consumption can be achieved by a single-dose of etoricoxib before induction of anesthesia
Detailed Description: Patients undergoing transabdominal hysterectomy were randomized to a group taking a single dose orally of etoricoxib 120 mg n 18 etoricoxib 180 mg n 17 or placebo n 15 2 hours before surgery under the same standardized general anesthesia At the post-anesthetic care unit intravenous morphine titration was given before starting self-controlled analgesia PCA device Morphine consumption pain relief score sedative score global evaluation score and side-effects were recorded at 1 2 4 8 and 24 h post-operatively The primary end points were morphine consumption within 24-hr post-operatively and total pain relief over 8 h TOPAR8 Patient global satisfaction was also assessed

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
Faculty of MedicineKhonKaenU None None None