Status:
COMPLETED
The Effects of Acupressure Applied to the Primiparous During Episiotomy
Lead Sponsor:
Esra SABANCI BARANSEL
Conditions:
Episiotomy Wound
Pain
Eligibility:
FEMALE
18+ years
Phase:
NA
Brief Summary
This study was conducted to determine the effects of acupressure applied during episiotomy repair on pain and anxiety levels of the primiparous. The study was conducted as a randomized controlled tri...
Detailed Description
Introduction: This study was conducted to determine the effects of acupressure applied during episiotomy repair on pain and anxiety levels of the primiparous. Methods: The study was conducted as a ra...
Eligibility Criteria
Inclusion
- Being 18 or older,
- having a single healthy newborn,
- Giving spontaneous birth through a medio-lateral episiotomy incision,
- No signs of infection such as vaginal redness or swelling,
- Women with full and healthy tissue integrity in the area where acupressure will be applied.
Exclusion
- The need to use unusual lidocaine during episiotomy repair (lidocaine 2% higher than 5 ml),
- having any postpartum complications (such as bleeding, hypertension).
Key Trial Info
Start Date :
June 1 2023
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 30 2023
Estimated Enrollment :
126 Patients enrolled
Trial Details
Trial ID
NCT06552104
Start Date
June 1 2023
End Date
December 30 2023
Last Update
September 27 2024
Active Locations (1)
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1
Esra Sabancı baransel
Malatya, Malatya, Turkey (Türkiye), 44280