Arthritis Clinical Trial
Official title:
Total vs. Reverse Shoulder Replacement: a Prospective Randomized Trial
NCT number | NCT01884077 |
Other study ID # | 201209102 |
Secondary ID | |
Status | Terminated |
Phase | N/A |
First received | |
Last updated | |
Start date | November 2012 |
Est. completion date | June 2016 |
Verified date | November 2018 |
Source | Washington University School of Medicine |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Specific Aim: To compare early postoperative pain relief in patients over the age of 70 who
undergo either Total Shoulder Arthroplasty or Reverse Shoulder Arthroplasty in treatment of
glenohumeral osteoarthritis.
Hypothesis: Early postoperative pain relief will be greater in those undergoing Reverse
Shoulder Arthroplasty.
Status | Terminated |
Enrollment | 19 |
Est. completion date | June 2016 |
Est. primary completion date | January 28, 2015 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 70 Years to 95 Years |
Eligibility |
Inclusion Criteria: - age 70 or older, - have radiographic signs of osteoarthritis (narrowing of the glenohumeral joint space, marginal osteophytes around the humeral head, progressive changes with sclerosis and subcortical cystic formation and flattening of the humeral head), - intact rotator cuff but with atrophy or fatty degeneration (defined as Grade II atrophy noted on preoperative shoulder ultrasound), - objective weakness as measured with Isobex testing, - limited forward elevation (less than 90 degrees) Exclusion Criteria: - patients who present with pain secondary to inflammatory arthropathy, - obvious full-thickness rotator cuff tear, - cuff tear arthropathy, - revision arthroplasty, - fracture or trauma, - patients who had previous rotator cuff repair or prior open surgery prior to shoulder arthroplasty. - pregnancy |
Country | Name | City | State |
---|---|---|---|
United States | Washington University School of Medicine | Saint Louis | Missouri |
Lead Sponsor | Collaborator |
---|---|
Washington University School of Medicine | Zimmer Biomet |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | ASES Score | American Shoulder & Elbow Survey (ASES): Assessment of patient-rated shoulder pain and function/disability. Questions involve activities of daily living that reflect the use of the shoulder & elbow in different planes of motion. Pain and weakness with various activities are also addressed. ASES score will be calculated, compared and reported for both groups pre-operatively and 2 years post operatively: (17 patients) total arthroplasty and (17 patients) reverse arthroplasty. | 2 years after shoulder replacement | |
Primary | WOOS Score | a disease-specific quality-of-life instrument (Western Ontario Osteoarthritis of the Shoulder [WOOS]. WOOS Score will be generated for both groups pre-operatively and 2 years post operatively: Reverse arthroplasty(17 patients) and Total arthroplasty (17 patients) Study has been discontinued |
2 years after shoulder replacement | |
Secondary | Shoulder Strength and Motion Based on Physican Examination | Research team member measures both shoulder range of motion (using a goniometer) and strength based on the standardized American Shoulder and Elbow Surgeons Society (ASES)examination. Physical Examination includes the following: forward elevation, external rotation, internal rotation, external rotation at side, Internal rotation extension with lift off exam, Horn Blower's, external rotation strength, thumb down abduction strength, abdominal compression test, Biceps rupture, Speeds Test, and Yergason's Test. External and Thumb Down abduction are measured with Iso-Force machine. Preoperative and 2 year post-operative range of motion and strength measurement score averages will be compared and reported for both groups (total 34 patients). | 2 years post shoulder replacement |
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