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Vaginal Birth After Caesarean Section - Effect on Maternal Psychosocial Function

Vaginal Birth After Caesarean Section - Effect on Maternal Psychosocial Function

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00517140
Enrollment
262
Registered
2007-08-16
Start date
2003-09-30
Completion date
2007-04-30
Last updated
2011-06-16

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

Conditions

Cesarean Section, Pregnancy, Uterine Rupture

Keywords

Pregnancy women with a scarred uterus due to previous caesarean section

Brief summary

The incidence of caesarean section has reached 15-20% in most developed countries. Encouraging vaginal birth after caesareans section (VBAC) has been considered a key component of a strategy to reduce the caesarean section rate. Most medical literature has focused on the efficacy of VBAC in reducing the caesarean section rate and the physical safety of successful VBAC. However, 30%-40% of these women fail to achieve a vaginal delivery. Little is known about how the uncertainty of labour outcome and a failed VBAC impact on the psychosocial function of these women. We propose to study a cohort of women with a prior caesarean section and presenting with a subsequent pregnancy for care. After consent and recruitment, these subjects will be randomly assigned to have a repeat caesarean section or VBAC. The medical outcomes, overall satisfaction of the subjects with the care they received, and the short-term psychosocial function of these subjects will be studied. The result of this study will provide important information that would be useful in assisting women to decide the mode of delivery after a prior caesarean section.

Interventions

PROCEDURERepeat Caesaen section
PROCEDUREvaginal delivery

Sponsors

Chinese University of Hong Kong
CollaboratorOTHER
Hospital Authority, Hong Kong
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE

Inclusion criteria

All women who: * Have one prior caesarean section * No prior vaginal delivery and * Agree for either vaginal delivery or elective caesarean section

Design outcomes

Primary

MeasureTime frame
pscyiatric morbidityafter delivery

Secondary

MeasureTime frame
Psychosocial function3 and 6 months after delivery

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026