lidocaine spray, pomade and infiltrative form in episiotomy repair
Phase 4
Completed
- Conditions
- The pain of the episiotomy
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 300
Inclusion Criteria
1. Pregnant women aged 18-40.
2. Women who have 37-42 weeks of pregnancy.
3. Women with nulliparous pregnancy.
4. Pregnant women with BMI <35.
5. Pregnant women who agree to participate in the study.
6. Pregnant women with postpartum obstetric episiotomy.
Exclusion Criteria
1. Multiparity.
2. Women with BMI> 35.
3. Women who have had vaginal surgery before.
4. Women who do not want to participate in the study.
5. Preterm births.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie lidocaine's analgesic effects in episiotomy repair?
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What combination therapies with lidocaine are being explored for postpartum pain management?