MedPath

Effect of Phenytoin cream on episiotomy wound healing and relif pai

Not Applicable
Conditions
Perineal wound care.
Disruption of perineal obstetric wound
Registration Number
IRCT201108243027N9
Lead Sponsor
Research Deputy of Tabriz university of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
120
Inclusion Criteria

Full term pregnancy; being nulliparous; no special diet;age 18-35 years; no specific diseases (cardiovascular, hepatic, renal; diabetes; coagulopathy diseases;anemia, no history of skin diseases; persistent constipation and hemorroids); mul-nutrition;not taking specific drugs ( such as anticoagulant;anti depressants;anti epileptic;antibiotics;immuno-suppressive drugs); no smoking and alcohol and drugs; having literacy; non- obese (BMI<29; according to the same scale);anterior fetal presentation;Episiotomy on gynecological bed;Episiotomy repair by chromic catgut sutures after prep and drep using the same techniques and in less than 30 minutes;visible injury or previous surgery in the perineal region;normal pregnancy;subjects' willingness to participate in the study;
Exclusion criteria: Hematomas or infection after the delivery; history of perineal and vaginal surgery;mismatch between maternal pelvis and fetal size (based on pelvis examination);disorders in labor (first stage of labor after 14 h;the second stage more than 2 h); prolonged rupture of amniotic sac (more than 18 h); manual placenta removal;manipulation of the perineum; excessive bleeding after childbirth; need for neonated resuscitation; extended Episiotomy;use of delivery aids;non- persistent use of drugs; women who decide to withdraw from the research.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Episiotomy wound healing. Timepoint: 24 hours and 10 days after delivery. Method of measurement: REED SCALE (Redness, echimosses, edema discharge, aproximation).
Secondary Outcome Measures
NameTimeMethod
Episiotomy pain relief. Timepoint: 24 hours and 10 days after intervention. Method of measurement: VAS scale(vissual analog scale).
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