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NCT00584272 Clinical Trial

Retrospective Study on the Outcome of Cleft Palate Repair: Comparing US Surgical and Ethicon Suture Materials

Cleft Palate Clinical Trial

Official title:
Retrospective Study on the Outcome of Cleft Palate Repair: Comparing US Surgical and Ethicon Suture Materials

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00584272
Other study ID # 200715210
Secondary ID
Status Completed
Phase N/A
First received December 26, 2007
Last updated June 19, 2017
Start date March 2007
Est. completion date April 2015

Study information
Verified date June 2017
Source University of California, Davis
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Investigator initiated retrospective chart review to study the effects of changing suture material on the healing and outcome of cleft palate surgery were.

Description:

This study aims to show what the effects of changing suture material were on the healing and outcome of cleft palate surgery. The study will be considered successful if we find that either there is an effect on the healing after surgery, one of the suture materials seems to promote better healing and final outcome, or that there is no difference between the suture materials.

Recruitment information / eligibility
Status Completed
Enrollment 88
Est. completion date April 2015
Est. primary completion date April 2015
Accepts healthy volunteers No
Gender All
Age group 1 Year to 10 Years
Eligibility Inclusion Criteria:

- Cleft palate repair performed at UCDMC between 1/1996 and 6/2006

Exclusion Criteria:

- Those who do not meet the inclusion criteria

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States University of California Davis Medical Center Sacramento California

Sponsors (1)
Lead Sponsor Collaborator
University of California, Davis

Country where clinical trial is conducted

United States, 

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