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Angle of progression and vaginal delivery

Angle of progression and vaginal delivery - APRO

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON43662
Enrollment
250
Registered
2016-02-25
Start date
2016-03-22
Completion date
Unknown
Last updated
2024-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

normal birth vaginal delivery

Interventions

None listed

Sponsors

Universitair Medisch Centrum Groningen
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
Main endpoint includes a cut-off for the angle of progression predicting successful vaginal delivery and successful vacuum delivery.

Secondary

MeasureTime frame
Secondary parameters include the results of the questionnaires evaluating the experiences of women in labor undergoing ITU.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)