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Efficacy of 3 foley catheter balloons side-by-side vs 1 balloon for labour induction at Princess Marina Hospital; a randomised control trial

Efficacy of 3 foley catheter balloons side-by-side vs 1 balloon for labour induction at Princess Marina Hospital; a randomised control trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
PACTR
Registry ID
PACTR202603863999452
Enrollment
88
Registered
2026-03-25
Start date
2026-03-01
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Induction of labor

Interventions

Three foley balloon catheters
One foley balloon catheter

Sponsors

University of Botswana
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Age 18 or more years Nulliparous or Multiparous No major medical complications Singleton, cephalic presentation, EFW < 4KG Prior unsuccessful labour induction may be included Gestational age at least 34 weeks and above

Exclusion criteria

Exclusion criteria: Previous cesarian delivery Urgent labour inductions indications (Eclampsia, Pre eclampsia, ruptured membranes) Declined consent

Design outcomes

Primary

MeasureTime frame
Vaginal birth within 48 hours after labour induction with no use of uterotonic labour augmentation and Apgar score >6 at 5 minutes

Secondary

MeasureTime frame
Vaginal birth within 24 hours after labour induction with no use of uterotonic labour augmentation and Apgar score >6 at 5 minutes;Caesarean birth;Use of uterotonic labour augmentation;Uterine hyperstimulation;Meconium stained liquor;Apgar score <7 at 5 minutes;Postpartum haemorrhage;Vaginal birth within 24 hours

Countries

Botswana

Contacts

Public ContactLeatile Sedabadi

Junior Lecturer

leatilesedabadi@gmail.com+26772455552

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026