Topical lidocaine and pain reduction in natural childbirth
Phase 2
Recruiting
- Conditions
- atural Vaginal Delivery.Single spontaneous delivery
- Registration Number
- IRCT20231025059855N1
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 54
Inclusion Criteria
Healthy pregnant women with first natural delivery
Gestational age between 37 and 41 weeks
Episiotomy incision below 5 cm
Patient satisfaction
Exclusion Criteria
Heavy bleeding during childbirth
The need to use a vacuum during delivery
Grade 3 and 4 perineal lacerations
History of previous allergy to lidocaine or prilocaine
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Intensity of pain. Timepoint: After the episiotomy and 1, 2, 4 and 24 hours after the episiotomy. Method of measurement: Visual Analogue Scale.;Patient satisfaction rate. Timepoint: After the episiotomy and 1, 2, 4 and 24 hours after the episiotomy. Method of measurement: Oral questionnaire.
- Secondary Outcome Measures
Name Time Method