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Rotator Cuff Surgical Outcomes in Women | Clinical Trials | Clareo Health

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UNKNOWNNCT02725320

Rotator Cuff Surgical Outcomes in Women

The overall purpose of this work is to use a prospective cohort study to examine patient-specific but shoulder-extrinsic factors and how they influence the results of rotator cuff surgery. There are u...

Lead sponsor: University of Calgary•1 locations•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

University of Calgary

Age

35 - 75 years

Sex

ALL

Healthy Volunteers

No

Inclusion Criteria

•Referred for surgical treatment of predominantly unilateral rotator cuff syndrome

Exclusion Criteria

•unable to speak or read English
•unable to complete 12 month follow-up
•significant cervicogenic arm and shoulder pain in the affected arm
•significant chronic pain diagnoses felt at least as likely to be the cause of the symptoms as the rotator cuff condition as evaluated by the surgeon

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: April 26, 2019Terms

Trial snapshot

StatusUNKNOWN

Phase—

Enrollment192

Start dateFeb 2016

Last updatedApr 26, 2019

Condition

Injury of Shoulder Region Rotator Cuff Syndrome

Locations shown

South Health Campus

Calgary, Alberta

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: April 26, 2019Data synced to Clareo: July 13, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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