4cm vs 5cm vs 6cm active phase of labour trial
Not Applicable
Not yet recruiting
- Conditions
- Pregnancy and Childbirth
- Registration Number
- PACTR202305811094904
- Lead Sponsor
- DR ILIKANNU SAMUEL OKWUCHUKW
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Female
- Target Recruitment
- 132
Inclusion Criteria
1.Willingness and consent to participate in the study
2.Nulliparity
3.Singleton viable intrauterine pregnancy
4.Term gestation (37-42weeks)
5.Active phase of labour (4cm or 5cm or 6cm)
6.Intact membranes
7.Cephalic presentation
Exclusion Criteria
1.Any contraindication to vaginal delivery
2.Multiple pregnancy
3.Ruptured membrane
4.Multiparas
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What are the clinical outcomes of using 4cm, 5cm, and 6cm cervical dilatation criteria for diagnosing active phase labor in nulliparous women?
How does the timing of intervention during active labor phase affect maternal and neonatal outcomes in first-time pregnancies?
What biomarkers correlate with cervical dilatation progression rates in nulliparous women during active labor?
Are there adverse events associated with delayed recognition of active labor phase using higher cervical dilatation thresholds?
How does this trial's approach to active labor diagnosis compare with current WHO guidelines for nulliparous women?