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Clinical Trial Summary

The aim of this study was to evaluate the relationship between perineal body length and perineal laceration risk in primigravid patients.

Primigravid women with singleton pregnancies in the first stage of labor at the 35th week of gestation were included in the study. The peineal body length of the patients was measured by the same physician.


Clinical Trial Description

After 35 weeks of gestation, nulliparous women with single gestation were included in the study and genital hiatus and perineal body measurements were taken.

The presence and degree of perineal laceration after birth were determined. Correlation of genital hiatus and perineal body measurements with perineal laceration risk were evaluated.

After birth, vaginal laceration, oxytocin use, fetal birth weight, the presence of episiotomy were recorded. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03880552
Study type Observational
Source Kanuni Sultan Suleyman Training and Research Hospital
Contact
Status Completed
Phase
Start date December 1, 2018
Completion date June 1, 2019

See also
  Status Clinical Trial Phase
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Enrolling by invitation NCT04616170 - The Patient Positioning for Perineal Protection Study N/A
Completed NCT03287258 - Perineal Preparation for Pregnant Ladies. N/A