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-2h84gt
- Lead Sponsor
- Escola de Enfermagem da Universidade de São Paulo
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruitment completed
- 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.
Do not have vaginal delivery; Not having first degree laceration with indication of suture; Have episiotomy or laceration of second, third or fourth degree; Have physometry; have vulvar varicose veins; Have complications from the childbirth or postpartum requiring hospital transfer of the woman to a hospital of high complexity.
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
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