Investigating the effect of Great Plantain and Damask Rose gel on wound

Investigating the effect of Great Plantain and Damask Rose gel on the episiotomy wound healing process

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20240806062673N1

Enrollment

Registered

2024-09-07

Start date

2024-08-22

Completion date

Unknown

Last updated

2024-09-16

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

Conditions

Episiotomy wound.

Interventions

Intervention 1: Intervention group: The medicine is in the form of a skin gel that contains plant extracts of great plantain and damask rose, and the colleagues of the Pharmaceuticals Department in Ya

Eligibility

Sex/Gender

Female

Age

18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Women older than 18 years and less than 45 years old Pregnancy age more than 37 weeks Normal vaginal Delivery Episiotomy wound

Exclusion criteria

Exclusion criteria: Excessive bleeding that requires a blood transfusion Obvious abnormality in the baby Extending the episiotomy incision to the anus Having diseases that interfere with wound healing Psychological stress such as death of parents, wife, baby

Design outcomes

Primary

Measure	Time frame
Wound healing process. Timepoint: Days 7 and 14 after the start of the intervention. Method of measurement: REEDA Score.;Perineal pain. Timepoint: Days 7 and 14 after the start of the intervention. Method of measurement: Visual analog scale of pain.	—

Secondary

Measure	Time frame
The degree of wound edema. Timepoint: Days 7 and 14 after the start of the intervention. Method of measurement: REEDA Score.;The extent of wound erythema. Timepoint: Days 7 and 14 after the start of the intervention. Method of measurement: REEDA Score.;The degree of wound ecchymosis. Timepoint: Days 7 and 14 after the start of the intervention. Method of measurement: REEDA Score.;Approximation of wound. Timepoint: Days 7 and 14 after the start of the intervention. Method of measurement: REEDA Score.;The amount of wound discharge. Timepoint: Days 7 and 14 after the start of the intervention. Method of measurement: REEDA Score.	—

Measure

Time frame

The degree of wound edema. Timepoint: Days 7 and 14 after the start of the intervention. Method of measurement: REEDA Score.;The extent of wound erythema. Timepoint: Days 7 and 14 after the start of the intervention. Method of measurement: REEDA Score.;The degree of wound ecchymosis. Timepoint: Days 7 and 14 after the start of the intervention. Method of measurement: REEDA Score.;Approximation of wound. Timepoint: Days 7 and 14 after the start of the intervention. Method of measurement: REEDA Score.;The amount of wound discharge. Timepoint: Days 7 and 14 after the start of the intervention. Method of measurement: REEDA Score.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRoghaye Zare

Yazd University of Medical Sciences

drzare313@gmail.com+98 35 3630 3062

Outcome results

None listed

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