Phytochemical investigations on myrtle and chamomlie essential oils and their effects on episiotomy

Phase 2

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

• Registration Number: IRCT20180707040370N7
• Lead Sponsor: Hamedan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 6 March 2024

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 120

Inclusion Criteria

Gestational age 37 weeks and higher at delivery time
Maternal age 18-35 years
Mediolateral incision and episiotomy degree 2
No physical diseases
No pregnancy complications
No condyloma or herpes lesions in the perineum
Primigravida

Exclusion Criteria

Infection during treatment
Irregular use of the drug
Refuse from continuing to participate in study

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain severity. Timepoint: Pre intervention, 6 hour and 5 and 10 days after intervention. Method of measurement: Visual analogue scale (VAS).;Healing wound. Timepoint: Pre intervention, 6 hour and 5 and 10 days after intervention. Method of measurement: Episiotomy wound healing rate scale, REEDA (Redness, Edema, Ecchymosis, Discharge, Approximation).