Clinical Trials Directory

Trials / Terminated

TerminatedNCT02247648

Efficacy of Extended-release, Once Daily Tramadol for Post Operative Analgesia in Shoulder Arthroscopy

Efficacy of Extended-release, Once Daily Tramadol for Post Operative in Ambulatory Shoulder Arthroscopy

Status
Terminated
Phase
Phase 2
Study type
Interventional
Enrollment
100 (actual)
Sponsor
Centre hospitalier de l'Université de Montréal (CHUM) · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Accepted

Summary

The investigators hypothesize that the use of tramadol will reduce pain and analgesic consumption after arthroscopic shoulder surgery.

Detailed description

The purpose of the study was to evaluate the efficacy of tramadol long acting for post operative pain in patients who had an arthroscopic shoulder surgery in ambulatory setting in comparison with a placebo. The intensity of pain was evaluated on a visual analog scale as the quantity of hydromorphone taken by patients, and the side effects during the first 72 hours.

Conditions

Interventions

TypeNameDescription
DRUGtramadolPatients from tramadol group received tramadol 100 mg day one, 100 mg day 2, and 200 mg day 3
DRUGPlaceboPatients from control group received a "shame" tramadol pill on day one, two, and 3

Timeline

Start date
2013-06-01
Primary completion
2017-12-01
Completion
2017-12-01
First posted
2014-09-25
Last updated
2020-07-24

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT02247648. Inclusion in this directory is not an endorsement.