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The effect of Quercus persica L and Lawsonia inermis L ointment on episiotomy wound healing in primiparous women in 2014-2015

The effect of Quercus persica L and Lawsonia inermis L ointment on episiotomy wound healing in primiparous women in 2014-2015

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015060122521N1
Enrollment
160
Registered
2015-06-27
Start date
2014-02-20
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

Condition 1: Infection of obstetric surgical wound. Condition 2: Haematoma of obstetric wound. Condition 3: Dehiscence of episiotomy wound. Infection of obstetric surgical wound Haematoma of obstetric wound Disruption of perineal obstetric wound

Interventions

Intervention 1: 5% Lawsonia inermis Cream, 1 cm, Twice per day, 10 days. Intervention 2: Placebo (Osirin) Cream, 1 cm, Twice per day, 10 days. Intervention 3: 2% Quercus persica Cream, 1 cm, Twice per
Treatment - Drugs
Placebo
5% Lawsonia inermis Cream, 1 cm, Twice per day, 10 days
Placebo (Osirin) Cream, 1 cm, Twice per day, 10 days
2% Quercus persica Cream, 1 cm, Twice per day, 10 days

Sponsors

Shahrekord University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: Nullipar (Gravid 1); Pregnancy age 37-42 weeks; Singleton fetus; Not Using special drugs as Glucocorticoids, Anticoagulant, Chemotherapy, Suppression of the immune or Radiotherapy; No disease history as impair the healing of chronic diseases such as systemic, heart, renal, Pulmonary, Coagulopathy, Immunocompromised, Connective tissue disorders, Diabetes, Anemia, Mental, Persistent constipation, Hemorrhoids, Hemophilia; Malnutrition; Sensitivity to herbal medicines; BMI between 19.8 to 26; Active skin disease such as allergic disorders; Scar or skin allergy; BV symptoms Exclusion Criteria: History reconstructive surgery on perineal; Failure to comply with the fetus in the mother's pelvis, pelvic examination; Interfere with the progress of labor (first stage more than 20 hours or second stage more than 2 hours or Cervical dilatation more than 5 cm per hour Fast Vaginal delivery); Manual removal of placenta; 3rd and 4th degree perineal tear; Prolonged rupture of membrane (more than 18 hours); Using of vacuum and forceps; abnormal bleeding or hematoma after delivery; Genital Warts; use irregularly ointment

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Wound Healing. Timepoint: Days 7, 10 and 14. Method of measurement: Reeda Scale.;Edema. Timepoint: Days 7, 10 and 14. Method of measurement: Reeda Scale.;Bruising. Timepoint: Days 7, 10 and 14. Method of measurement: Reeda Scale.;Secretion. Timepoint: Days 7, 10 and 14. Method of measurement: Reeda Scale.;Distance between edges of wound. Timepoint: Days 7, 10 and 14. Method of measurement: Reeda Scale.;Redness. Timepoint: Days 7, 10 and 14. Method of measurement: Reeda Scale.

Secondary

MeasureTime frame
Pain Intensity. Timepoint: Days 7, 10 and 14. Method of measurement: Pain Perception Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Sanaz Zibanejad

Shahrekord University of Medical Sciences

Zibanejad@skums.ac.ir+98 38 3222 0016

Outcome results

None listed

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