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Evaluation the effect of Malva sylvestris L extract ointment on pain intensity and incision of during delivery wound healing in primiparous women

Comparison of the effect of Malva sylvestris L extract ointment and placebo on pain intensity and episiotomy wound healing in primiparous women

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20100130003226N19
Enrollment
112
Registered
2022-11-28
Start date
2023-01-21
Completion date
Unknown
Last updated
2023-02-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Episiotomy. Perineal laceration during delivery

Interventions

Intervention 1: Intervention group: Intervention group: Uses 3% Malva sylvestris L ointment for 10 days (daily) at a rate of two centimeters, on episiotomy wound. This ointment is produced at the Facu

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Married women aged 18 to 35 years primiparous Being Iranian Gestational age between 37 to 42 weeks No smoking, alcohol and drugs Being literate in reading and writing Having a single fetus with cephalic presentation Fetal weight between 2500 and 4000 gr Body Mass Index (BMI) between 18.5 and 25 Vaginal delivery with mediolateral episiotomy The normality of the first, second and third stages of labor

Exclusion criteria

Exclusion criteria: Amniotic sac rupture more than 24 hours Allergy to Malva sylvestris L ointment Having fever, puerperal infection and hematoma Infant hospitalization at Neonatal Intensive Care Unit Having postpartum hemorrhoids or fissures Having sex in the first ten days after delivery

Design outcomes

Primary

MeasureTime frame
Episiotomy wound healing. Timepoint: Before the intervention, the first 24 hours, 5 and 10 days after treatment. Method of measurement: REEDA scale assess 5 items such as Redness, Edema, Ecchymoses, Discharge from the wound and Approximation of the perineal tissues.;Episiotomy wound pain intensity. Timepoint: Before the intervention, the first 24 hours, 5 and 10 days after treatment. Method of measurement: The visual pain scale (VAS) is a tool for measuring the intensity of pain, which is a 10 cm ruler with eleven numbers.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahrokh Dolatian

Shahid Beheshti University of Medical Sciences

mhdolatian@gmail.com+98 21 8865 5366

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026