Viewing Study NCT06484192



Ignite Creation Date: 2024-07-17 @ 11:59 AM
Last Modification Date: 2024-10-26 @ 3:33 PM
Study NCT ID: NCT06484192
Status: ENROLLING_BY_INVITATION
Last Update Posted: 2024-07-03
First Post: 2024-06-26

Brief Title: Pain Control After Lumbar Spine Fusion
Sponsor: Rothman Institute Orthopaedics
Organization: Rothman Institute Orthopaedics

Study Overview

Official Title: Randomized Controlled Trial of Postoperative Inpatient Ketorolac and Outpatient Naproxen Use Following Elective Lumbar Spine Fusion
Status: ENROLLING_BY_INVITATION
Status Verified Date: 2024-06
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: The purpose of this randomized controlled trial is to determine if patients who receive non-steroidal anti-inflammatory medications NSAIDs following elective lumbar spinal fusion have increased rates of symptomatic nonunion requiring revision spinal surgery at two-years follow-up compared to those who do not receive NSAIDs
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: True
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: True
Is an FDA AA801 Violation?: None