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

Not Applicable
Conditions
Episiotomy.
First degree perineal laceration during delivery
Registration Number
IRCT201604256888N14
Lead Sponsor
Research Ethics Committee of Hamadan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
70
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

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
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.
Secondary Outcome Measures
NameTimeMethod
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