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The effect of Olea ointment and Lidocaine Gel 2 % on pain relieving and episiotomy wound healing

Phase 2
Recruiting
Conditions
Episiotomy.
First degree perineal laceration during delivery,Second degree perineal laceration during delivery
O70.0, O70
Registration Number
IRCT2017020332374N1
Lead Sponsor
Guilan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
123
Inclusion Criteria

Inclusion criterias: Iranian patients; Primiparous; 18-35 years old; Literate; Volunteer; Term pregnancy with single fetus; Cephalic presentation; Mediolateral episiotomy; Newborn weight about 2500-4000 g; Absence of diseases affecting wound healing; Lack of PROM longer than 18 hours; The maternal BMI range between 19/8 and 30.
Exclusion criteria: Unwillingness to continue to participate in the study; The use of other effective drugs for wound healing during the study; Inappropriate use of medications (more than two nights); Allergy to the Olea ointment or Lidocaine gel 2%; Failure to go to hospital on days 5 and 10 after delivery; Having a sexual relationship in the first five days after childbirth.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Severity of episiotomy pain. Timepoint: Before intervention; 2 h and 24 h after first intervention; 5th and 10th days of postpartum. Method of measurement: pain visual scale.;Episiotomy wound healing. Timepoint: Before intervention; 2 h and 24 h after first intervention; 5th and 10th days of postpartum. Method of measurement: REEDA Scale.
Secondary Outcome Measures
NameTimeMethod
Drug side effects. Timepoint: 2h after first intervention; 24h after first intervention; 5th and 10th days of postpartum. Method of measurement: Drug side effects Form.;Maternal health condition. Timepoint: 2h after first intervention; 24h after first intervention; 5th and 10th days of postpartum. Method of measurement: Maternal health condition Form.;Used analgesic. Timepoint: 2h after first intervention; 24h after first intervention; 5th and 10th days of postpartum. Method of measurement: Used analgesic Form.
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