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NCT04633837: ECM

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

Terminated NA Results posted Last updated 6 January 2022
What this trial tests

NA trial testing Extracellular Matrix Graft Injectable Implant in Arthroscopic Shoulder Surgery in 15 participants. Terminated before completion.

Timeline
4 December 2020
Primary endpoint
7 November 2021
7 November 2021

Quick facts

Lead sponsorBrian Badman
PhaseNA
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposetreatment
Enrollment15
Start date4 December 2020
Primary completion7 November 2021
Estimated completion7 November 2021
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Brian Badman

Who can join

Adults 18 to 55, any sex, with Arthroscopic Shoulder Surgery or Pain, Postoperative. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Arthroscopic Shoulder Surgery

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04633837.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing