Clinical Trials Logo

Clinical Trial 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. What we do know is that antenatal depression and unplanned caesarean section are major risk factors for postpartum depression, which in turn is the major cause of maternal mortality in many developed countries including Hong Kong. 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. The Hypothesis is that there is a significant difference in psychosocial function between these 2 groups of patients.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00294411
Study type Interventional
Source Chinese University of Hong Kong
Contact
Status Completed
Phase N/A
Start date December 2003

See also
  Status Clinical Trial Phase
Recruiting NCT05091944 - An Interactive Web-based Birth Decision Aid for Shared Decision Making N/A
Recruiting NCT05246761 - Balloon Catheter Combined With Oxytocin Induction Among the Pregnant Women With Previous Cesarean Section
Recruiting NCT05215041 - The Effectiveness and Safety of the Trial of Labor in Full Term Pregnant Women With Cesarean Section After Spontaneous Labor
Completed NCT03098966 - Evaluation of Trials of Labor After Previous Cesarean Section in Ain Shams University Maternity Hospital N/A
Not yet recruiting NCT05996926 - Diagnostic Accuracy of Saline Sonohystrography vs. 3D Transvaginal Ultrasound for Cesarean Scar Defect Assessment N/A
Completed NCT04053413 - University of North Carolina-Healthwise Partnership Project on Birth Options Decision Aid N/A