Angle of progression and vaginal delivery

Completed

• Conditions: normal birth; vaginal delivery; 10010273

• Registration Number: NL-OMON43662
• Lead Sponsor: niversitair Medisch Centrum Groningen

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 23 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 250

Inclusion Criteria

1. Nulliparous and multiparous women.
2. Singleton pregnancy.
3. Age >=18 years and good understanding of the Dutch language.
4. At term gestation (37 weeks or more).
5. Fetus in cephalic presentation.
6. Second stage of labor.

Exclusion Criteria

1. Cesarean section or instrumental vaginal delivery performed solely because of suspected fetal distress.
2. Delivery elsewhere than the University delivery ward.

Study & Design

• Study Type: Observational invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Main endpoint includes a cut-off for the angle of progression predicting<br /><br>successful vaginal delivery and successful vacuum delivery.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Secondary parameters include the results of the questionnaires evaluating the<br /><br>experiences of women in labor undergoing ITU.</p><br>