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Effect of olive leaf extract ointment on pain intensity and healing wound of episiotomy

Effect of olive leaf extract ointment on pain intensity and healing wound of episiotomy in Primiparous women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015062422908N1
Enrollment
90
Registered
2015-08-02
Start date
2015-05-04
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

episiotomy. Disruption of perineal obstetric wound

Interventions

Intervention 1: The intervention group: Olive leaf extract ointment 3 times a day for 10 days (preparation and packaging by Dana kasian Khorram Abad company) as much as one finger (equivalent to 1 gr
Treatment - Drugs
Placebo
The intervention group: Olive leaf extract ointment 3 times a day for 10 days (preparation and packaging by Dana kasian Khorram Abad company) as much as one finger (equivalent to 1 gram) will be used
The placebo group: Placebo ointment 3 times a day for 10 days (preparation and packaging by Dana kasian Khorram Abad company) as much as one finger (equivalent to 1 gram) will be used locally on the
Control group: 10% betadine solution of 3 tablespoons in 4 glasses of water , 3 times a day for 10 days will be used for sitz bath.

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
17 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria contain: Age between 17 to 35 years, Age between 17 to 35 years; Primiparous women; Normal vaginal delivery; Full term singleton pregnancy with cephalic presentation; Gestational age between 37 to 42 weeks; Medio-lateral episiotomy without extending the incision and tear of grade 3 and 4; Body mass index <30; Absence of reconstructive surgery in the perineal area; Absence of illness, Not using drugs effecting on wound healing . Exclusion criteria: Failure to use the correct and consistent command of ointment; Abnormal vaginal bleeding after delivery; Postpartum perineal manipulation; Episiotomy infection; The need for episiotomy stitches this location; Sensitivity to ointments .

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain intensity. Timepoint: 4 hours after delivery (first day after delivery) ,3 days after delivery,7 days after delivery, 10 days after delivery,14 days after delivery. Method of measurement: Visual Analouge Scale.;Healing of episiotomy. Timepoint: 4 hours after delivery (first day after delivery) ,3 days after delivery,7 days after delivery, 10 days after delivery,14 days after delivery. Method of measurement: REEDA scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaasumeh Kaviani

Shiraz University of Medical Scienses

kavianimaasumeh@yahoo.com kavianm@sums.ac.ir+98 71 3647 4251

Outcome results

None listed

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