Viewing Study NCT00092378



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Last Modification Date: 2024-10-26 @ 9:10 AM
Study NCT ID: NCT00092378
Status: COMPLETED
Last Update Posted: 2017-05-09
First Post: 2004-09-22

Brief Title: A Study of Two Approved Drugs in the Treatment of Post-Bunionectomy Surgery Pain 0966-234COMPLETED
Sponsor: Merck Sharp Dohme LLC
Organization: Merck Sharp Dohme LLC

Study Overview

Official Title: A Randomized Double-Blind Placebo- and Active-Comparator-Controlled Parallel-Group Study of Rofecoxib and Diclofenac Sodium in the Treatment of Post-Bunionectomy Surgery Pain
Status: COMPLETED
Status Verified Date: 2017-05
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: This purpose of this study is to compare the safety and effectiveness of two approved drugs in the treatment of pain following bunionectomy surgery
Detailed Description: The duration of treatment is 5 days for rofecoxib and 1 day for diclofenac sodium

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
2004_072 None None None