RECRUITING

Nonopioid Analgesia After Labral Surgery

Conditions

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

This is a randomized, single blinded, standard of care controlled clinical trial. This project aims to compare postoperative pain control in patients in two treatment arms of rotator cuff repair: a treatment group given a nonopioid pain control regimen, and a standard of care control group given standard opioid pain control regimen

Official Title

Traditional vs. Nonopioid Analgesia After Labral Surgery

Quick Facts

Study Start:2019-01-22
Study Completion:2020-05-20
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT03825809

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:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * All adult patients over age 18 and scheduled for a primary or revision labral surgery
  1. * Exclusion criteria will include patients with a medical history of known allergies or intolerance to allergies or intolerance to Celebrex, Tylenol, Neurontin, dexamethasone, tramadol, substantial alcohol or drug abuse, and pregnancy, history of narcotics within 6 months of surgery, renal impairment, peptic ulcer disease, GI bleeding. Secondary exclusion criterion is an intact rotator cuff

Contacts and Locations

Study Contact

Toufic R Jildeh, MD
CONTACT
517-230-8511
tjildeh1@hfhs.org

Principal Investigator

Toufic R Jildeh, MD
PRINCIPAL_INVESTIGATOR
Henry Ford Health System

Study Locations (Sites)

Henry Ford Health System
Detroit, Michigan, 48202
United States

Collaborators and Investigators

Sponsor: Henry Ford Health System

  • Toufic R Jildeh, MD, PRINCIPAL_INVESTIGATOR, Henry Ford Health System

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 Date2019-01-22
Study Completion Date2020-05-20

Study Record Updates

Study Start Date2019-01-22
Study Completion Date2020-05-20

Terms related to this study

Additional Relevant MeSH Terms

  • Narcotic Use