The Use of St. John's Wort Oil With Massage in the Perineum During Childbirth
NCT ID: NCT05164926
Last Updated: 2024-07-31
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
60 participants
INTERVENTIONAL
2023-05-15
2024-12-30
Brief Summary
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The investigators'aim in this study is to investigate the effects of perineal massage with St. John's Wort oil on episiotomy, perineal damage and wound healing.
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Detailed Description
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The control group will consist of 30 pregnant women who were applied perineal massage without using centaury oil as a requirement of midwifery care service.
The rates of 3rd and 4th degree perineal damage will be recorded from the groups that received St. John's Wort oil after delivery and those who did not. The current cut-out size and depth and its localization will also be recorded. At the same time, the patient will be evaluated for VAS for postpartum perineal pain.
In the follow-up one week after discharge, the scar thickness and pelvic muscle strength assessment of the existing episioes and eruptions will be recorded. The presence of urinary or fecal incontinence will be recorded by asking.
The data will be saved in the IBM-SPSS program. When comparing the two groups, normally distributed data will be analyzed using the independent simple t test, and data not normally distributed will be analyzed using the Mann-Whitney U-Test. P value less than 0.05 will be considered significant.
Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Experimental group, whose perineum was massaged with St. John's Wort oil during labor
St. John's Wort oil will be applied to this group during perineal massage during labor.
perineal massage with St. John's Wort oil
perineal massage with St. John's Wort oil during labor
Interventions
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perineal massage with St. John's Wort oil
perineal massage with St. John's Wort oil during labor
Eligibility Criteria
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Inclusion Criteria
* active labor during the examination
* pregnant woman who is likely to have a vaginal delivery
Exclusion Criteria
18 Years
40 Years
FEMALE
Yes
Sponsors
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Ankara City Hospital Bilkent
OTHER
Responsible Party
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Rahime Bedir Fındık
Associate Professor Dr
Principal Investigators
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Rahime Bedir Findik, Dr
Role: PRINCIPAL_INVESTIGATOR
Ankara City Hospital Bilkent
Locations
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Rahime Bedir Findik
Ankara, Çankaya, Turkey (Türkiye)
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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AnkaraCHBilkent-MH-RBF-02
Identifier Type: -
Identifier Source: org_study_id
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