process of labor in women with female genital mutilation / cutting

Not Applicable

• Conditions: Female genital mutilation labor process

• Registration Number: PACTR201901521518882

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2018-12-02
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 400

Inclusion Criteria

1. Women aged 18-45
2. Women with previous female circumcision (RTE EAH)
3. Pregnant women who have not undergone female genital mutilation (Trabzon Kanuni EAH)
4. Women with BMI <35
5. Women who agree to participate in the study
6. Pregnant women with nulliparity
7. Women with 37-42 weeks of pregnancy

Exclusion Criteria

1. Women with BMI> 35
2. Women who have undergone previous vaginal surgery
3. Women who do not want to participate in the study
4. multiparity

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Visual analogue pain score and axiality score will be applied to patients at both centers at the beginning of labor. During the labor, the pain score will be re-examined in the active phase.

Secondary Outcome Measures

Name	Time	Method
All labor processes in the delivery room (delivery week, 1st stage of delivery, latent and active phase duration, duration of 2nd stage, duration of 3rd stage, episiotomy and obstetric tears, amount of bleeding, The amount of hemoglobin before and after birth, maternal and fetal complications, fetus intensive care need, weight and apgar score) will be recorded.