Trial · NCT04037683
qMOLI- A Qualitative Assessment of Misoprostol or Oxytocin for Labour Induction
NCT04037683, Completed, University of Liverpool
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. qMOLI- A Qualitative Assessment of Misoprostol or Oxytocin for Labour Induction. Trials, record NCT04037683. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04037683
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- qMOLI- A Qualitative Assessment of Misoprostol or Oxytocin for Labour Induction
- NCT number
- NCT04037683
- Status
- Completed
- Enrollment
- 136 participants, actual
- Lead sponsor
- University of Liverpool
- Conditions
- Pre-Eclampsia
- Interventions
- Misoprostol Oral Tablet, Oxytocin
- First posted
- 2019-07-30
- Last updated
- 2022-02-11
Source ClinicalTrials.gov
Registered outcomes5
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Patients' views on induction of labour, prior to induction. | 6 months | Explore patients' perceptions of induction of labour, prior to induction. |
| Primary | Patients' views on induction of labour, post induction. | 6 months | To explore the experiences of patients post induction and any differences between the two RCT groups; misoprostol/misoprostol vs misoprostol/oxytocin regimes. |
| Primary | Clinicians' views on various induction protocols. | 6 months | To better understand the acceptability of the different induction regimes to health care professionals. To explore potential barriers for implementing research findings into clinical practice and potential solutions. |
| Primary | Patients' views on the fetal monitoring regimens during the induction process. | 6 months | To explore patients' perspectives of the fetal monitoring regimens during the induction process. |
| Primary | Staff's views on the fetal monitoring regimens during the induction process. | 6 months | To explore staff perspectives of the fetal monitoring regimens during the induction process. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers1
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as |
|---|---|
| 40912733 | DERIVED |
Source PubMed
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT04037683
GET https://conductscience.org/api/trials/v1/NCT04037683/registered