Clinical trial the effect of Hypericum Perforatum (Perforan) on wound healing episiotomy in wome

Not Applicable

• Conditions: Episiotomy during vaginal delivery.; Disruption of wound of; episiotomy

• Registration Number: IRCT201505061557N5
• Lead Sponsor: Vice Chancellor for research of Arak University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

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

Inclusion Criteria

singleton pregnancy;primiparous; episiotomy
Exclusion criteria: severe infection in 5th day after episiotomy; any acute or chronic diseases or allergy to Hypericum Perforatum

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: Before intervention, 5 and 10 day after intervention. Method of measurement: visual analogue scale.;Discharge. Timepoint: Before the intervention, 5 and 10 days after the intervention. Method of measurement: Presence of suppurative vaginal discharge.;Remained sutures. Timepoint: Before the intervention, 5 and 10 days after the intervention. Method of measurement: number of remained sutures.;Dehiscence. Timepoint: 10th day after intervention. Method of measurement: Incidence of wound dehiscence.;Edema. Timepoint: Before the intervention, 5 and 10 days after the intervention. Method of measurement: Diameter of edema on wound site in Centimiter.;Redness. Timepoint: Before the intervention, 5 and 10 days after the intervention. Method of measurement: Diameter of redness in millimeter.

Secondary Outcome Measures

Name	Time	Method
Infection. Timepoint: Before the intervention, 5 and 10 days after the intervention. Method of measurement: Presence of infective discharge and dehiscence of wound.