RECRUITING

The Effect of Multimodal Pain Regimen on Use of Narcotics After Rotator Cuff Tear Repair

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The goal of this clinical trial is to understand which group of pain control medications work best in adults after rotator cuff surgery.

Official Title

The Effect of Multimodal Pain Regimen on Use of Narcotics After Rotator Cuff Tear Repair

Quick Facts

Study Start:2025-07

Study Completion:2025-12

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT07076069

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
* Adults with rotator cuff tears who have failed conservative therapy and undergoing arthroscopic rotator cuff repair.	* Patients without capacity to consent for the study * Patients not able to have local nerve block * Patients who underwent previous shoulder surgery on the same side, kindling revision rotator cuff repair * Patients who are unable to record and verbalize their pain level due to altered mental status * Patients who are unable to tolerate any of the medications included in the multimodal pain regimen or standard pain regimen due to severe allergies or inability to consume medication * Patients with history of previously diagnosed alcohol or drug abuse, renal impairment, peptic ulcer disease, and gastrointestinal bleeding * Patients who are pregnant

Inclusion Criteria

Exclusion Criteria

* Adults with rotator cuff tears who have failed conservative therapy and undergoing arthroscopic rotator cuff repair.

* Patients without capacity to consent for the study
* Patients not able to have local nerve block
* Patients who underwent previous shoulder surgery on the same side, kindling revision rotator cuff repair
* Patients who are unable to record and verbalize their pain level due to altered mental status
* Patients who are unable to tolerate any of the medications included in the multimodal pain regimen or standard pain regimen due to severe allergies or inability to consume medication
* Patients with history of previously diagnosed alcohol or drug abuse, renal impairment, peptic ulcer disease, and gastrointestinal bleeding
* Patients who are pregnant

Contacts and Locations

Study Contact

Ferdinand Chan, M.D.

CONTACT

718-920-2060

fchan@montefiore.org

Principal Investigator

Ferdinand Chan, M.D.

PRINCIPAL_INVESTIGATOR

Montefiore Medical Center

Study Locations (Sites)

Montefiore Hutchinson Campus

Bronx, New York, 10461

United States

Collaborators and Investigators

Sponsor: Montefiore Medical Center

Ferdinand Chan, M.D., PRINCIPAL_INVESTIGATOR, Montefiore Medical Center

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-07

Study Completion Date2025-12

Study Record Updates

Study Start Date2025-07

Study Completion Date2025-12

Terms related to this study

Additional Relevant MeSH Terms

Rotator Cuff Repairs
Pain Management