aser Treatment for pain relief in Cesarean operative wound

Not Applicable

• Conditions: Care post operative, cesarean, women.; E04.520.252.500; M01.975; E02.760.731.700

• Registration Number: RBR-6b8hcc
• Lead Sponsor: Departamento de Fisioterapia da Universidade Federal do Rio Grande do Norte

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2017-10-03
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruitment completed
• Sex: Female
• Target Recruitment: Not specified

Inclusion Criteria

8 to 10 hours postpartum cesarean; Pain on the numerical scale of pain greater or equal 3 in the region of the cesarean incision; Without clinical or obstetrical intercurrences; Without infectious process; Receive the same drug treatment (anti-inflammatory, analgesic and old) with equal interval of ingestion.

Exclusion Criteria

Women who do not accept to perform the intervention with the low intensity laser; Puerpera with difficulty of communication and expression; Volunteers who present clinical and obstetric instability during the data collection.

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Effect of low intensity laser therapy for surgical incision pain relief in women submitted to cesarean section comparing 4 groups after three evaluations (at the beginning, middle and end of collection) with appraise blinded. The first evaluation performed in the puerpera who was 8 to 12 hours postpartum cesarean. The second evaluation was performed 24 hours after the first evaluation. The third evaluation was carried out.

Secondary Outcome Measures

Name	Time	Method
ow intensity laser therapy with effect of improvement in the painful symptoms of the puerperas, pain threshold of the puerperas, perception of improvement of the pain after intervention.The digital algometer will be used, a scale of global perception of improvement and evaluation with the numerical scale of pain in the evalutions. The first evaluation performed in the puerpera who was 8 to 12 hours postpartum cesarean. The second evaluation was performed 24 hours after the first evaluation. The third evaluation was carried out.