The effect of chamomilla cream on wound healing and pain of episiotomy in Primiparous wome

Not Applicable

• Conditions: wound healing of episiotomy , pain of episiotomy.; Disruption of perineal obstetric wound

• Registration Number: IRCT2013051413336N1
• Lead Sponsor: Research Council of Mashhad 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: 106

Inclusion Criteria

nulliparous women aged 18-35 years old living in the city of Mashhad, Iran; at least having the ability to read and write; living with his wife's; body mass index ranging from 19/8-30; non-smoking and no drug dependence; no history of disease impaired wound healing; not using drugs effecting on wound healing; single fetal cephalic; lack of symptomatic infections of the vagina and vulva (the infectious discharge, itching, burning); low blood, anal lesions; vulva and perineum on admission; and rupture of the fetal sac up to 12 hours before the start of pains; lack of stricture restriction pelvic; embryos is vital; the lack of apparent anomalies in the newborn. No rectocel, cystocele severe (grade 2 or higher), wall or mass in the vaginal; no history of obstetric complications, use of acetaminophen suppository in 6 hours before delivery; no history of vaginal reconstructive surgery on the Vagina and urethra
Exclusion criteria: there interfere with the progress of labor; prolonged second stage of labor longer than 2 hours; delivery devices (vacuum, forceps); delivered via cesarean section; extend the length of the incision or there tear except episiotomy tear; infant hospitalization in the NICU; abnormal vaginal bleeding; shoulder dystocia (leading to the maneuvers other than Robert Mack); manual removal of placenta; hematoma; having intercourse to the end of the study (15 days postpartum); curettage procedure the first 24 hours after birth; the third stage of labor longer than 30 minutes; the occurrence of an adverse event at 15 days postpartum; no need for episiotomy; not use the cream on a regular; puerperal fever; complications resulting from the use of chamomile cream.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain of episiotomy. Timepoint: Immediately before the intervention to 2 weeks after intervention. Method of measurement: McGill Pain Questionnaire short.;Wound healing of episiotomy. Timepoint: First Day of episiotomy repair to 14 days. Method of measurement: Scale reeda.

Secondary Outcome Measures

Name	Time	Method
The rate of pain episiotomy. Timepoint: Immediately prior to the 2-week after the start of the intervention intervention. Method of measurement: Questionnaire McGill Pain short.;The rate of wound healing of episiotomy. Timepoint: First Day of episiotomy repair to 14 days. Method of measurement: Scale reeda.