CAS: Changes in Anthropometry Following Ambulatory Orthopaedic Surgery

• Sponsor: State University of New York at Buffalo (Other)
• Overall Status: Withdrawn
• CT.gov ID: NCT02435251
• Collaborator: (none)
• Enrollment: 0
• Location: 1
• Duration (Months): 27
• Patients Per Site Per Month: 0

Study Details

Study Description

Brief 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.

Condition or Disease	Intervention/Treatment	Phase
Knee Surgery; Shoulder Surgery	Device: dual energy X-ray absorptiometry

Study Design

• Study Type: Observational
• Actual Enrollment: 0 participants
• Observational Model: Case-Only
• Time Perspective: Prospective
• Official Title: Changes in Anthropometry Following Ambulatory Orthopaedic Surgery
• Study Start Date: Jan 1, 2014
• Actual Primary Completion Date: Apr 1, 2016
• Actual Study Completion Date: Apr 1, 2016

Outcome Measures

Primary Outcome Measures

1. Fat mass [6-weeks after surgery]

Secondary Outcome Measures

1. Lean mass [6-weeks after surgery]

2. Weight [6-weeks after surgery]

3. Body mass index [6-weeks after surgery]

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years to 70 Years
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

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

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	UBMD Orthopaedics & Sports Medicine	Amherst	New York	United States	14226

Sponsors and Collaborators

• State University of New York at Buffalo

Investigators

• Principal Investigator: Leslie Bisson, MD, University at Buffalo

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Leslie Bisson, June A. & Eugene R. Mindell, MD Professor and Chair, State University of New York at Buffalo
• ClinicalTrials.gov Identifier: NCT02435251
• Other Study ID Numbers: 458943-7
• First Posted: May 6, 2015
• Last Update Posted: Oct 23, 2019
• Last Verified: Oct 1, 2019

Study Results

No Results Posted as of Oct 23, 2019