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Subcutaneous Adaption and Cosmetic Outcome Following Caesarean Delivery

NCT01542346 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 116

Last updated 2013-07-15

No results posted yet for this study

Summary

This is a double blinded randomized study investigating if subcutaneous adaption has an impact on cosmetic outcome after Caesarean delivery.

Conditions

  • Caesarean Delivery

Interventions

PROCEDURE

subcutaneous adaption

Sponsors & Collaborators

  • Klinikum Klagenfurt am Wörthersee

    lead OTHER

Principal Investigators

  • Heinrich Husslein, M.D. · Klinikum Klagenfurt am Woerthersee and Medical University Vienna

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-03-31

Countries

  • Austria

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 NCT01542346 on ClinicalTrials.gov