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Use of Insorb Absorbable Vicryl Staples in Skin Closure for Cesarean Section

NCT01446627 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 300

Last updated 2013-05-03

No results posted yet for this study

Summary

The purpose of this study is to evaluate the incidence of wound breakdown or wound infection following skin closure with Insorb subcuticular absorbable staples versus metal staples after cesarean section through a retrospective chart analysis.

Conditions

  • Wound Infection

Interventions

OTHER

There is no intervention for this study

None, no intervention made.

Sponsors & Collaborators

  • The University of Texas Health Science Center, Houston

    lead OTHER

Principal Investigators

  • Jonathan P Faro, MD, PhD · UTHSC at Houston

Eligibility

Min Age
14 Years
Max Age
50 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-01-31
Primary Completion
2012-01-31
Completion
2012-12-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01446627 on ClinicalTrials.gov