Study To Evaluate Upper Arm Autologous Fat Transfer
Pilot Study To Evaluate Upper Arm Autologous Fat Transfer
1 other identifier
observational
10
1 country
1
Brief Summary
The objective of this pilot study is to observe the utility of autologous transfer of fat collected using ultrasonic assisted liposuction into the upper arms with ultrasonic visualization.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Mar 2011
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 1, 2011
CompletedFirst Submitted
Initial submission to the registry
March 9, 2011
CompletedFirst Posted
Study publicly available on registry
March 11, 2011
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2011
CompletedStudy Completion
Last participant's last visit for all outcomes
March 1, 2012
CompletedMarch 26, 2012
March 1, 2012
9 months
March 9, 2011
March 23, 2012
Conditions
Keywords
Study Arms (1)
Autologous fat transfer
Interventions
Autologous fat transfer from abdomen to upper arms
Eligibility Criteria
Male patients undergoing abdominal liposuction who wish autologous fat transfer to the upper arms
You may qualify if:
- Is male.
- Is between 20 and 50 years of age, inclusive, on the day of enrolment.
- Is to undergo abdominal liposuction.
- Wishes to undergo autologous fat transfer to the upper arms.
You may not qualify if:
- Currently enrolled in another device or drug study that has not completed the required follow-up period, or has completed all other study-required follow-up less than 30 days before enrolment in this study.
- Undergoing body contouring for reconstruction following injury or disease.
- Deemed inappropriate candidates for the surgical procedures for any reason.
- Are unwilling to undergo the study procedures or participate fully in all follow-up.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Dr David Matlock
Beverly Hills, California, 90069, United States
MeSH Terms
Conditions
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- INDUSTRY
Study Record Dates
First Submitted
March 9, 2011
First Posted
March 11, 2011
Study Start
March 1, 2011
Primary Completion
December 1, 2011
Study Completion
March 1, 2012
Last Updated
March 26, 2012
Record last verified: 2012-03