Trial · NCT05084534
Efficacy and Safety of Midodrine in Refractory or Recurrent Ascites in Children With Cirrhosis.
NCT05084534, Not applicable, Withdrawn, Institute of Liver and Biliary Sciences, India
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Efficacy and Safety of Midodrine in Refractory or Recurrent Ascites in Children With Cirrhosis. Trials, record NCT05084534. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT05084534
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Efficacy and Safety of Midodrine in Refractory or Recurrent Ascites in Children With Cirrhosis.
- NCT number
- NCT05084534
- Status
- Withdrawn
- Phases
- Not applicable
- Enrollment
- 0 participants, actual
- Lead sponsor
- Institute of Liver and Biliary Sciences, India
- Conditions
- Refractory Ascites in Children With Cirrhosis
- Interventions
- Midodrine, Standard medical treatment
- First posted
- 2021-10-19
- Last updated
- 2024-05-07
Source ClinicalTrials.gov
Registered outcomes14
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | • To compare the proportion of patients who will achieve partial or complete control of ascites at 12 weeks after therapy between the two groups | 12 weeks | |
| Secondary | • Comparison of total number of therapeutic paracentesis (>50ml/kg) procedures between the groups by the end of 12 weeks | 12 weeks | |
| Secondary | • Frequency of complete response (elimination of ascites) by 12 weeks | 12 weeks | |
| Secondary | • Time taken to achieve complete response | 12 weeks | |
| Secondary | • Frequency of partial response (persistent ascites not requiring therapeutic paracentesis) by 12 weeks | 12 weeks | |
| Secondary | • To compare change in plasma renin activity from baseline to 12 weeks | 12 weeks | |
| Secondary | • Change in serum sodium from baseline to 4 weeks and 12 weeks | 12 weeks | |
| Secondary | • Change in eGFR from baseline to 4 weeks | 4 weeks | |
| Secondary | • Change in MAP at 1 week, 4 weeks and 12 weeks from baseline | 12 weeks | |
| Secondary | • Comparison of proportion of patients with transplant free survival at 12 weeks between the 2 groups | 12 weeks |
1 to 10 of 14Source ClinicalTrials.gov
See all 14 registered outcomesOutcomes0
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/NCT05084534
GET https://conductscience.org/api/trials/v1/NCT05084534/registered