Trial · NCT04190173
Efficacy of PRUcalopride in Critically Ill Patients With Paralytic ILeus
NCT04190173, Phase 3, Unknown, Prince of Songkla University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Efficacy of PRUcalopride in Critically Ill Patients With Paralytic ILeus. Trials, record NCT04190173. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04190173
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Efficacy of PRUcalopride in Critically Ill Patients With Paralytic ILeus
- NCT number
- NCT04190173
- Status
- Unknown
- Phases
- Phase 3
- Enrollment
- 62 participants, estimated
- Lead sponsor
- Prince of Songkla University
- Conditions
- Paralytic Ileus, Critically Ill
- Interventions
- Prucalopride, Placebo
- First posted
- 2019-12-09
- Last updated
- 2020-02-06
Source ClinicalTrials.gov
Registered outcomes10
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change of maximum bowel diameter from baseline at 24 hours | after first dose intervention to next 24 hours | measure on plain abdominal radiography by blinded radiologist |
| Primary | Change of maximum bowel diameter from baseline at 48 hours | after first dose intervention to next 48 hours | measure on plain abdominal radiography by blinded radiologist |
| Primary | Change of maximum bowel diameter from baseline at 72 hours | after first dose intervention to next 72 hours | measure on plain abdominal radiography by blinded radiologist |
| Primary | Change of maximum bowel diameter from baseline at 96 hours | after first dose intervention to next 96 hours | measure on plain abdominal radiography by blinded radiologist |
| Primary | Change of maximum bowel diameter from baseline at 120 hours | after first dose intervention to next 120 hours | measure on plain abdominal radiography by blinded radiologist |
| Secondary | change of abdominal circumference from baseline at 24 hours | after first dose intervention to next 24 hours | measured at umbilical level |
| Secondary | change of abdominal circumference from baseline at 48 hours | after first dose intervention to next 48 hours | measured at umbilical level |
| Secondary | change of abdominal circumference from baseline at 72 hours | after first dose intervention to next 72 hours | measured at umbilical level |
| Secondary | change of abdominal circumference from baseline at 96 hours | after first dose intervention to next 96 hours | measured at umbilical level |
| Secondary | change of abdominal circumference from baseline at 120 hours | after first dose intervention to next 120 hours | measured at umbilical level |
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.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
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/NCT04190173
GET https://conductscience.org/api/trials/v1/NCT04190173/registered