Viewing Study NCT02029235


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Ignite Modification Date: 2026-01-05 @ 5:21 PM
Study NCT ID: NCT02029235
Status: TERMINATED
Last Update Posted: 2018-12-13
First Post: 2014-01-03
Is NOT Gene Therapy: True
Has Adverse Events: True

Brief Title: Post-operative Analgesia in Elective, Soft-tissue Hand Surgery
Sponsor: Alexander Payatakes, M.D.
Organization:

Study Overview

Official Title: Post-operative Analgesia in Elective, Soft-tissue Hand Surgery: A Randomized, Double Blind Comparison of Acetaminophen/Ibuprofen Versus Acetaminophen/Hydrocodone
Status: TERMINATED
Status Verified Date: 2018-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Early termination due to slower than anticipated recruitment.
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 research study is to find out which combination of pain medications following surgery work the best and result in the fewest side effects.
Detailed Description: This is a prospective, randomized, double-blind study comparing the efficacy of acetaminophen/hydrocodone (AH) to acetaminophen/ibuprofen (AIBU) in providing adequate post-operative pain relief in elective, soft tissue hand surgery patients.

Study Oversight

Has Oversight DMC: False
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?: