Examining the Effectiveness of a Connective Tissue Matrix Implant in Reducing Post-operative Pain and Narcotic After Outpatient Arthroscopic Shoulder Surgery

Stopped early · Not applicable

Conditions studied: Arthroscopic Shoulder Surgery, Pain, Postoperative

In brief

This document is a protocol for a human research study. This study is to be conducted according to United States standards of Good Clinical Practice in accordance with applicable Federal regulations and institutional research policies and procedures. Extracellular matrix grafts have been used to help with postoperative inflammation.

Key facts

Study ID

NCT04633837

Run by

Brian Badman

People needed

15

Starts

2020-12-04

Expected to finish

2021-11-07

Last updated by the study team

2022-01-06

Who can join

Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Age 18 and older
• Primary diagnosis of rotator cuff tear, labral tear or SLAP tear
• Able to provide informed consent
• Is willing and able to accept text messages

You may not qualify if…

• Older than 55 years old.
• Pregnancy.
• Known narcotic or alcohol abuse (< 3 months)
• Revision shoulder surgery
• Current narcotic regimen or contract with pain management specialist

Where it is running

• American Health Network — Avon, Indiana, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.