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Comparison of the effect of phenytoin Cream and Honey Cream on episiotomy pain and healing of episiotomy

Phase 2
Conditions
Episiotomy pain and wound healing.
Second degree perineal laceration during delivery
Registration Number
IRCT201405318801N8
Lead Sponsor
?Shahid Beheshti University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Other
Sex
Female
Target Recruitment
120
Inclusion Criteria

Term and Nulliparous Pregnancy; A literate, between 18-35 of age; race Persia; Living in Kashan; a live singleton fetus with cephalic presentation; birth weight between 2500-4000 grams; BMI In the range of 19.8 to 30; The lack of effect on wound healing drugs (anticoagulants, antidepressants, anticonvulsants, alcohol, glucocorticoids, suppression of the immune system, antibiotics and chemotherapy); narcotics and psychotropic drugs; Disturbing lack of healing diseases (chronic, systemic, cardiac, renal, pulmonary, coagulation disorders, immune deficiency, connective tissue disorders, diabetes, anemia, psychiatric disease, hemophilia, depression, malnutrition) and no history of injury, or previous surgery of lesions visible in the perineum (genital warts, hemorrhoids), persistent constipation; Lack PROM more than 18 hours; lack a history of reactions to local anesthetics or lidocaine; absence of bleeding after childbirth; lack of manual removal of the placenta; the absence of perineal hematoma; No manipulation of the perineum after delivery; failure or anomaly NICU baby; for more than 14 hours not take delivery of the first stage, second stage of labor greater than 2 hours to not take, the third stage of labor not take more than half an hour.

Exclusion Criteria

Drugs affecting the healing of wounds (anticoagulants, antidepressants, anticonvulsants, alcohol Glkvkvrtykvyydha, suppressing the immune system, antibiotics and chemotherapy) during the study; Not used regularly and as directed cream; creams desired sensitivity; lack of desire to continue participating in the study; having sex in the first five days after birth; coming to the clinic.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain Intensity. Timepoint: First 24 hours after delivery (baseline value) - Seven days after the intervention - fourteen days after the intervention. Method of measurement: Pain ruler.;Episiotomy wound healing. Timepoint: First 24 hours after delivery (baseline value) - Seven days after the intervention - fourteen days after the intervention. Method of measurement: Control by improving the perineum (the scale Reeda).
Secondary Outcome Measures
NameTimeMethod
Stiffness. Timepoint: First 24 hours after childbirth, the postpartum seventh day, the fourteenth day after delivery. Method of measurement: Questionnaire.;Irritation. Timepoint: First 24 hours after childbirth, the postpartum seventh day, the fourteenth day after delivery. Method of measurement: Questionnaire.;Itching. Timepoint: First 24 hours after childbirth, the postpartum seventh day, the fourteenth day after delivery. Method of measurement: Questionnaire.;Dryness. Timepoint: First 24 hours after childbirth, the postpartum seventh day, the fourteenth day after delivery. Method of measurement: Questionnaire.;Discharge from the wound. Timepoint: First 24 hours after childbirth, the postpartum seventh day, the fourteenth day after delivery. Method of measurement: Questionnaire.;Fever and chills. Timepoint: First 24 hours after childbirth, the postpartum seventh day, the fourteenth day after delivery. Method of measurement: Questionnaire.
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