MedPath

se of Infrared Laser in Vaginal Delivery

Not Applicable
Conditions
Healing of episiotomies.
E04.520.252.750
A01.719
G08.686.702
Registration Number
RBR-9zxb97
Lead Sponsor
Financiamento Próprio - Bolsa Mestrado do CAPES
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruitment completed
Sex
Female
Target Recruitment
Not specified
Inclusion Criteria

Healthy women aged over 18 years. With term pregnancy (between 37 and 41 weeks and 6 days of gestation). Without previous vaginal birth. Having had spontaneous delivery with mediolateral episiotomy without perineal laceration. Episiorrhaphy performed with catgut simple. Single fetus in cephalic presentation and live. Not presenting an infectious disease, hemorrhoids, bruising or varicose veins in vulva-perineal region. Did not have any preparation of the perineal area during pregnancy. Do not use drugs photosensitising endogenous or exogenous. Not present clinical or obstetric complications.

Exclusion Criteria

Use any product in vulva-perineal region, other than soap and water.

Study & Design

Study Type
Intervention
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Episiotomy healing will be evaluated before the three irradiations and 7 to 10 days after after discharge, with a numerical scale that quantifies the redness, edema ,ecchymosis, discharge and approximation of wound edges (Scale REEDA- Redness Edema Echymosis Discharge Aproximation).
Secondary Outcome Measures
NameTimeMethod
The intensity of pain will be evaluated by numerical scale from 0 to 10, with 0 is equal to no pain and 10 is the maximum pain. The evaluation will be done before and 30 minutes after irradiations.<br>
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