The effect of Zingiber officinale on healing and pain of episiotomy

Not Applicable

Recruiting

• Conditions: Disruption of perineal obstetric wound; Episiotomy.; O90.1

• Registration Number: IRCT20110922007618N9
• Lead Sponsor: Tabriz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 7 September 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 70

Inclusion Criteria

Primiparous women
The lack of drug and psychotropic
Age range 35-18 years
Birth of a live, single fetus
Do not use any special medicine(such as anti-inflammatory drugs other than acetaminophen and coagulation based on the patient's statements)
history of impaired wound healing disease, like systemic disease, cardiac, renal, pulmonary, coagulation disorders, immune deficiency, connective tissue disorders, diabetes,haemophilia
Failure to follow the special diet
No anemia during pregnancy
The lack of early PPH
No history of prenatal vaginal examinations and manipulations
extent or large episiotomy (repair length 4-3 cm)
Willingness and possibility for the mother to visit Al-Zahra Hospital on days 5 and 10
No history of reconstructive surgery on the vagina and intercostals (according to the woman)
Lack of long-term rupture of the amniotic sac (more than 18 hours)
Do not use blood pressure medications (mothers with high blood pressure and preeclampsia)
Do not use topical lidocaine cream
Do not use mopericin
Do not use curettage in mothers

Exclusion Criteria

Unwillingness to participate in the study

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Episiotomy wound healing. Timepoint: Before intervention,12 hours after delivery and on days 5 and 15. Method of measurement: Epidatomic wound healing scale; REEDA (Redness, Edema, Ecchymosis, Discharge, Approximation).;The severity of episiotomy pain. Timepoint: Before intervention,12 hours after delivery and 5 and 15 days later. Method of measurement: Visual Pain Scale (vas).

Secondary Outcome Measures

Name	Time	Method
Count the acetaminophen pills used. Timepoint: Fifteenth day after delivery. Method of measurement: Counting tablets.;The frequency of side effects in the group receiving ginger extract ointment ginger and placebo. Timepoint: Fifteenth day after delivery. Method of measurement: Questionnaire.