Evaluation of the effectiveness of Adhesive Tissue in the skin and mucosa of Perineal Tears
- Conditions
- First degree perineal laceration during deliveryWomenO70.0M01.975
- Registration Number
- RBR-52y5tq
- Lead Sponsor
- Thaís Trevisan Teixeira
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- Female
- Target Recruitment
- Not specified
to have up to 6 centimetres of cervical dilation at the time the woman is invited to participate in the research; Do not use steroid substances; Do not present leucorrhoea or any signs of infection at the repair site; No diagnosis of diabetes mellitus; without history of allergy to surgical glue or formaldehyde; No difficulty in understanding the Portuguese language or in communication; Accept being submitted to perineal repair methods with skin adhesive or suture thread.
to have up to 6 centimetres of cervical dilation at the time the woman is invited to participate in the research; Do not use steroid substances; Do not present leucorrhoea or any signs of infection at the repair site; No diagnosis of diabetes mellitus; without history of allergy to surgical glue or formaldehyde; No difficulty in understanding the Portuguese language or in communication; Accept being submitted to perineal repair methods with skin adhesive or suture thread.
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Decrease of the intensity of perineal pain, verified through the Visual Numerical Scale (from 0 to 10 where 0 represents absence of pain and 10 the worst possible pain), considering the decrease of 2 or more points in the mean of the experimental group, related to the control group. The outcome will be assessed in the following moments after birth: until 2 hours, 12-24 hours, 36-48 hours and 10-20 days.
- Secondary Outcome Measures
Name Time Method