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Abdominoplasty Under Epidural Anesthesia

This study has been completed.
Sponsor:
Information provided by:
Rambam Health Care Campus
ClinicalTrials.gov Identifier:
NCT01389635
First received: July 6, 2011
Last updated: July 7, 2011
Last verified: July 2011
  Purpose

Abdominoplasty is one of the most popular body-contouring procedures, yet it is also among the most hazardous aesthetic procedures currently performed. It was shown, in many studies, to be associated with a significant complication rate, some of which are life-threatening. This study describes the investigators experience with a series of abdominoplasties performed under epidural anesthesia. Outcomes are presented, especially in terms of complication, and the practical advantages of this method are discussed.


Condition
Abdominoplasty

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Retrospective
Official Title: Abdominoplasty Under Epidural Anesthesia: Safer for the Patient, Easier for the Surgeon.

Further study details as provided by Rambam Health Care Campus:

Enrollment: 31
Study Start Date: March 2009
Study Completion Date: April 2009
Primary Completion Date: March 2009 (Final data collection date for primary outcome measure)
Groups/Cohorts
Abdominoplasty patients
All patients who underwent abdominoplasty at our institution without concurrent operations

  Eligibility

Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population

All patients that underwent abdominoplasty between January 2003 and March 2008 in a private hospital by Dr. Yitshak Ramon.

Criteria

Inclusion Criteria:

  • All patients that underwent abdominoplasty between January 2003 and March 2008 in a private hospital by Dr. Yitshak Ramon.

Exclusion Criteria:

  • Patients with concurrent operations requiring general anesthesia.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01389635

Locations
Israel
Elisha Medical Center
Haifa, Israel
Sponsors and Collaborators
Rambam Health Care Campus
Investigators
Principal Investigator: Yitshak Ramon, MD Plastic Surgery Department, Rambam Healthcare Campus
  More Information

No publications provided

Responsible Party: Professor Yehuda Ullmann, Head, Department of Plastic Surgery, Rambam Healthcare Campus
ClinicalTrials.gov Identifier: NCT01389635     History of Changes
Other Study ID Numbers: 0019-11-RMB-CTIL
Study First Received: July 6, 2011
Last Updated: July 7, 2011
Health Authority: Israel: Ministry of Health

Keywords provided by Rambam Health Care Campus:
Abdominoplasty
Epidural

ClinicalTrials.gov processed this record on November 20, 2014