THE PAIN IN EPISIATOMY SITE.
Conditions
Interventions
Intervention 1: Intervention group: Lidocaine with clove oil Control group: Lidocaine. In the intervention group, in the lidocaine group (control), its injectable form (lidocaine 2%) and in the interv
Sponsors
Tehran University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 35 Years
Inclusion criteria
Inclusion criteria: Single and primiparous or second pregnancies the age range of 18 to 35 years, live fetus the gestational age 38 to 42 weeks, no medical problems before and after delivery, no specific drug or food allergies, no special problems such as abnormalities, disorder In the development of dilatation and effusion, do not use forceps and vacuum for childbirth
Exclusion criteria
Exclusion criteria: thwe women who dont need episiatomy such as high quallity of skin and muscle in prineoum
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Episiotomy pain. Timepoint: Measurements at the beginning of the study (before an episiotomy incision) and during wound healing. Method of measurement: visual pain assessment questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactElham Ebrahimi
Tehran University of Medical Sciences
Outcome results
None listed