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qMOLI- A Qualitative Assessment of Misoprostol or Oxytocin for Labour Induction — qMOLI  

Pre-Eclampsia Clinical Trial

Official title:
An Alongside Qualitative Study Exploring Patients' and Health Care Professionals' Expectations and Experiences of Labour Induction With Misoprostol and Oxytocin for Hypertension in Pregnancy in India

Clinical Trial Summary

Q MOLI is an alongside qualitative study, for the 'Misoprostol or Oxytocin for Labour Induction' (MOLI) pragmatic, open-label, randomised controlled trial, comparing a misoprostol/misoprostol regime vs the standard misoprostol/oxytocin induction of labour regime.1000 patients with hypertensive disease in pregnancy will be recruited, over 24 months, in Nagpur, India.

Clinical Trial Description

Qualitative study involving semi-structured interviews, with participants (pregnant women with hypertension/pre-eclampsia participating in the 'Misoprostol or Oxytocin for Labour Induction' (MOLI) study who consent to enter the qualitative study) in a randomised trial, pre and post induction of labour and focus group discussions with healthcare professionals involved in the study (MOLI study staff; practitioners who are involved in screening, recruiting, randomising and consenting participants to the MOLI study). The investigators aim to assess the priorities, experiences and acceptability of women being induced for hypertension in pregnancy in India, and clinician's views on the feasibility, usability, acceptability and barriers to implementation of various induction protocols. 1. Explore patients' perceptions, expectations, priorities, understanding of and concerns around induction of labour, prior to induction. 2. To explore the experiences, acceptability and satisfaction of patients post induction and any differences between the two RCT groups; misoprostol/misoprostol vs misoprostol/oxytocin regimes. 3. To better understand the feasibility, usability and acceptability of the different induction regimes to health care professionals. To explore potential barriers for implementing research findings into clinical practice and potential solutions. 4. To explore patients' and staff perspectives of the fetal monitoring regimens during the induction process. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04037683
Study type Observational
Source University of Liverpool
Contact
Status Completed
Phase
Start date October 18, 2019
Completion date December 31, 2021
View Details
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