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The effect of Aloevera gel on prineal pain & wound healing after episiotomy in primi para women

The effect of Aloevera gel on prineal pain & wound healing after episiotomy in primi para women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201604256888N14
Enrollment
70
Registered
2016-07-11
Start date
2016-07-22
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. First degree perineal laceration during delivery

Interventions

Intervention 1: Patients in the intervention group: will be treated with aloe gel-Barij Essence product- twice daily for 10 days. Intervention 2: Group control: will be treated with routine treatment
Treatment - Drugs
Patients in the intervention group: will be treated with aloe gel-Barij Essence product- twice daily for 10 days.
Group control: will be treated with routine treatment for 10 days.

Sponsors

Research Ethics Committee of Hamadan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: primiparus? having single pregnancy, episiotomy without rupture and without using device? gestational age between 37-42 weeks? No history of systemic diseases such as chronic diseases, cardiovascular disease, respiratory disease, connective tissue coagulation disorders, diabetes, anemia, immune deficiency and ... ? The absence of allergy or hypersensitivity (allergic) reactions to topical medication in the past? The lack of underlying disease, eclampsia, and preeclampsia in pregnancy? No rupture of membranes more than 24 hours? lack of prolonged labor? Lack of drug addiction? lack of vulvar and vaginal symptoms of inflammation, a normal BMI? Having mediolateral episiotomy and stitches it with the size of 3-5 cm and separate and cut Goth thread, number zero Exclusion criteria: not taken properly (Aloe Vera) after delivery? the incidence of allergy (rash, redness and swelling) and infections? incidence of new trauma for any reason at length study

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: 10 days after delivery. Method of measurement: VAS ruler.;Edema. Timepoint: 10 days after delivery. Method of measurement: visual.;Redness. Timepoint: 10 days after delivery. Method of measurement: visual.;Ecchymosis. Timepoint: 10 days after delivery. Method of measurement: visual.;Discharge. Timepoint: 10 days after delivery. Method of measurement: visual.;Approximation. Timepoint: 10 days after delivery. Method of measurement: visual.;Sexual function. Timepoint: 6 up to 12 weeks after delivery. Method of measurement: FSFI questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Shobeiri

Hamadan University of Medical sciences

shobeiri@umsha.ac.ir+98 81 3827 6051

Outcome results

None listed

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