Trial · NCT01200732
Phosphodiesterase-5 Inhibitor in Eisenmenger Syndrome
NCT01200732, Phase 2, Completed, Govind Ballabh Pant Hospital
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Phosphodiesterase-5 Inhibitor in Eisenmenger Syndrome. Trials, record NCT01200732. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01200732
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Phosphodiesterase-5 Inhibitor in Eisenmenger Syndrome
- NCT number
- NCT01200732
- Status
- Completed
- Phases
- Phase 2
- Enrollment
- 28 participants, actual
- Lead sponsor
- Govind Ballabh Pant Hospital
- Conditions
- Eisenmenger Syndrome
- Interventions
- Tadalafil, placebo
- First posted
- 2010-09-14
- Last updated
- 2010-09-14
Source ClinicalTrials.gov
Registered outcomes6
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | The primary end point of efficacy was improvement in exercise tolerance as assessed by the un-encouraged 6 minute walk test (6MWT) compared to baseline after 6 weeks of treatment | 6 weeks | |
| Secondary | The secondary endpoints were effect of the drug on systemic oxygen saturation (SaO2) | 6 weeks | |
| Secondary | The secondary endpoints were effect of the drug on effective pulmonary blood flow(EPBF) | 6 weeks | |
| Secondary | The secondary endpoints were effect of the drug on pulmonary vascular resistance (PVR). | 6 weeks | |
| Secondary | The secondary endpoints were effect of the drug on systemic vascular resistance (SVR) | 6 weeks | |
| Secondary | The secondary endpoints were effect of the drug on WHO functional class | 6 weeks |
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.
Papers2
The papers the trial lists on ClinicalTrials.gov.
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/NCT01200732
GET https://conductscience.org/api/trials/v1/NCT01200732/registered