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Use of Infrared Laser in Vaginal Delivery

Use of Infrared Laser in Vaginal Delivery with Episiotomy: Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-9zxb97
Enrollment
Unknown
Registered
2011-06-21
Start date
2011-05-01
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healing of episiotomies.

Interventions

Sample - 50 women divided into 2 groups (25 in the control group and 25 in the experimental group). Intervention - laser irradiation at low intensity in healthy women with episiotomies. Experimental g
Other
E02.594.540
E04.520.252.750

Sponsors

Financiamento Próprio - Bolsa Mestrado do CAPES
Lead Sponsor
Escola de Enfermagem da Universidade de São Paulo - EEUSP
Collaborator

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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.

Countries

Brazil

Contacts

Public ContactMarina Alvarenga

Escola de Enfermagem da Universidade de São Paulo

marinaobusp@gmail.com+55(11)97445-9213

Outcome results

None listed

Source: REBEC (via WHO ICTRP)