Warm compress on the injury severity of perineal pain in labor
Not Applicable
Completed
- Conditions
- Childbirth.Spontaneous vertex delivery
- Registration Number
- IRCT2012072410327N2
- Lead Sponsor
- Vice chancellor for research,sums
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 150
Inclusion Criteria
gestational age 37-42 weeks; primiparous; OA; single fetus; show vertex; no cpd; no history of any medical condition and no risk of preeclampsia.
Exclusion criteria: use of forceps or vacuum and prolonged second stage of delivery more than 2 hours.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Perineal trauma. Timepoint: After deliviry. Method of measurement: Chek list.;The pain od the second stage of labor. Timepoint: Immediately after deliveryand one day after delivery. Method of measurement: McGill ruller.
- Secondary Outcome Measures
Name Time Method The lenght of rupture. Timepoint: After intervention. Method of measurement: Centimeter.;Intensity of pain. Timepoint: Immediately after delivery and one day after delivery. Method of measurement: McGill ruler.
Related Research Topics
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What molecular mechanisms underlie perineal trauma during spontaneous vertex delivery in primiparous women?
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What are the potential adverse events associated with warm compress application during the second stage of labor?
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