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The effect of topical ointment of Propolis on severity of episiotomy pain and wound healing

The effect of topical ointment of Propolis on severity of episiotomy pain and wound healing: a randomized controlled trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20110524006582N37
Enrollment
72
Registered
2023-03-09
Start date
2023-03-13
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

Condition 1: Severity of episiotomy pain. Condition 2: Episiotomy wound healing.

Interventions

Intervention 1: Intervention group: Participants in the intervention group will use 2 cm (1 knuckle length) ointment on the ?Episiotomy site twice a day, 12 hours apart, for ten days. The contents of

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Gravid one and two women Living in Tabriz city Willingness and possibility of the mother to go to Alzahra and Taleghani hospitals on the 10th day Vaginal delivery with mediolateral incision

Exclusion criteria

Exclusion criteria: Prolonged rupture of the amniotic sac (more than 18 hours) Use of special drugs such as anti-inflammatory and anticoagulant drugs Addiction to alcohol or drugs History of diseases interfering with wound healing such as systemic, cardiac, renal, pulmonary diseases, coagulation disorder, immunodeficiency, connective tissue disorder, diabetes, anemia, mental illness, hemophilia (based on medical records) Abnormal postpartum bleeding Preterm labor Allergy to propolis Large or extended episiotomy (third or fourth degree tear and episiotomy cut length greater than 3-4 cm) History of surgery or visible lesions in the perineum Severe anemia (hemoglobin less than 7 grams per deciliter) Other tears in addition to episiotomy, such as urethral tears Non-continuing cooperation of participants Incomplete participation that is not possible to achieve results

Design outcomes

Primary

MeasureTime frame
Pain level of episiotomy. Timepoint: At the beginning of the study (before the start of the intervention) and on the 10th day after delivery. Method of measurement: Visual Analogue Scale.;Episiotomy wound healing rate. Timepoint: At the beginning of the study (before the start of the intervention) and on the 10th day after delivery. Method of measurement: Redness, Edema, Ecchymosis, Discharge, Approximation scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMasoomeh Rafat Nia

Tabriz University of Medical Sciences

Rafatniamasume@gmail.com+98 41 3478 5229

Outcome results

None listed

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