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NCT02435251 Clinical Trial

Changes in Anthropometry Following Ambulatory Orthopaedic Surgery

Shoulder Surgery Clinical Trial

— CAS  

Official title:
Changes in Anthropometry Following Ambulatory Orthopaedic Surgery

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT02435251
Other study ID # 458943-7
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date January 2014
Est. completion date April 2016

Study information
Verified date October 2019
Source State University of New York at Buffalo
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this research is to study changes in weight, body mass index, and percentage of fat following orthopaedic knee or shoulder surgery.

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date April 2016
Est. primary completion date April 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- 18-70 years-old

- scheduled to undergo knee or shoulder ambulatory surgery

Exclusion Criteria:

- weighs greater than 350 pounds

- pregnancy

- history of bariatric surgery

- dieting or engaged in a weight loss program

- taking weight loss supplements

- undergoing other types of surgery during study period

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• dual energy X-ray absorptiometry

Locations
Country Name City State
United States UBMD Orthopaedics & Sports Medicine Amherst New York

Sponsors (1)
Lead Sponsor Collaborator
State University of New York at Buffalo

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Fat mass 6-weeks after surgery
Secondary Lean mass 6-weeks after surgery
Secondary Weight 6-weeks after surgery
Secondary Body mass index 6-weeks after surgery
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