Clinical Trials Directory

Trials / Completed

CompletedNCT02839005

Absorbable Suture Versus Nonabsorbable Suture Intradermal for the Skin Transverse Section in Cesarean

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Universidade do Vale do Sapucai · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

Context: Cesarean section is the most common surgery in women, both in developed and underdeveloped countries. However results are conflicting report in which material for intradermal suturing get better aesthetic result. Objective: To compare the aesthetic appearance of two suture materials, polyglecaprone 25 and polyamide (nylon) with intradermal sutures for skin closure in women undergoing cesarean section first. Methods: This is a clinical, prospective and randomized study which was conducted in the Department of Gynecology and Obstetrics of a tertiary Institute, Hospital das Clinicas Samuel Libânio, in PousoAlegre, Estate of Minas Gerais. Sixty women undergoing cesarean section were first included and randomized into two groups: group I (n = 30) polyamide and group II (n = 30) polyglecaprone 25. Hypertrophy, color and width of the wound were evaluated, receiving a score, according to Trimbos table, six months after surgery. Later the results were compared to non-parametric statistical tests

Conditions

Interventions

TypeNameDescription
OTHERContinuous suture with polyglecaprone 25At the end of surgical procedemento of cesarean delivery , for skin closure continuous suture was performed with polyglecaprone 25
OTHERContinuous suture with polyamide (nylon)At the end of surgical procedemento of cesarean delivery , for skin closure continuous suture was performed with polyamide (nylon)

Timeline

Start date
2015-04-01
Primary completion
2016-01-01
First posted
2016-07-20
Last updated
2016-07-20

Locations

1 site across 1 country: Brazil

Source: ClinicalTrials.gov record NCT02839005. Inclusion in this directory is not an endorsement.