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wound episiotomy healing

Comparative impact of honey cream & cur cumin cream on episiotomy wound healing in primiparous women (clinical trial double) blind)

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT201108087257N1
Enrollment
Unknown
Registered
2011-09-11
Start date
2011-09-06
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 wound healing. Sequelae of complication of pregnancy, childbirth and the puerperium

Interventions

Intervention 1: Group 1: Use of honey topical on episiotomy wound BID/day for 10 days. Intervention 2: Group2: Use of corcomin topical on episiotomy wound BID/day for 10 days. Intervention 3: Group co
Treatment - Drugs
Placebo
Group 1: Use of honey topical on episiotomy wound BID/day for 10 days
Group2: Use of corcomin topical on episiotomy wound BID/day for 10 days
Group control: Use of placebo topical( topical base material without honey or corcomin) on episiotomy wound BID/day for 10 days

Sponsors

Babol University of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
17 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: primiparous women aged between 17-35 years; gestational age between 37-42 weeks; no smoking or useing drug; no history of disease impaired wound healing and not suffering from chronic systemic diseases Exclusion criteria: Median episiotomy; Perineal tear grade 3 and 4; infant in hospital admission and Irregular use of topical medications

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Episiotomy wound healing. Timepoint: Befor intervention(2 hours after stitching)-5 days after intervention(after delivery)- 10 days after intervention(after delivery). Method of measurement: REEDA scale (redness, edema, ecchymosis, discharge and approximation).

Secondary

MeasureTime frame
Preneal tear pain. Timepoint: Five and 10 days after intervention. Method of measurement: Visual analog scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSedigheh Smaelzadeh

Babol University Of Medical Siences

sesmael@yahoo.com+98 11 1223 8302

Outcome results

None listed

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