Trial · NCT03362047
(RIGHT HEART III Study - Right Ventricular Hemodynamic Evaluation and Response to Treatment)
NCT03362047, Phase 2, Completed, University of Giessen
3 sourcestrials-2026-11-12-0.4.0
Cite this record
ConductScience Library. (RIGHT HEART III Study - Right Ventricular Hemodynamic Evaluation and Response to Treatment). Trials, record NCT03362047. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03362047
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- (RIGHT HEART III Study - Right Ventricular Hemodynamic Evaluation and Response to Treatment)
- NCT number
- NCT03362047
- Status
- Completed
- Phases
- Phase 2
- Enrollment
- 7 participants, actual
- Lead sponsor
- University of Giessen
- Conditions
- Pulmonary Arterial Hypertension (PAH)
- Interventions
- Riciguat Group, Macitentan Group
- First posted
- 2017-12-05
- Last updated
- 2025-03-30
- Other registries' IDs
- eudract:2015-002835-17
Source ClinicalTrials.gov
Registered outcomes5
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | RV function | 12 weeks | Evaluation of the therapeutic effect of both treatment groups as measured by the change in systolic and diastolic RV function within 12 weeks after starting medication to plan a larger Phase II study. Methods: RV Catheterisation and Conductance Catherterisation. |
| Secondary | recruitability | 12 months | The feasible to include 30 patients within 12 months will be assessed by descripitve statistic |
| Secondary | feasibility to set up a larger phase II study | 24 months | The feasibility to set up a larger phase II study with this study setting and design will be assessed by descripitve statistic |
| Secondary | RV contractility | 12 weeks | Percent change in RV contractility (= end-systolic elastance, EES), RV, Methods: RV Catheterisation and Conductance Catherterisation. |
| Secondary | Collection of Adverse Events | 12 weeks | number of participants with adverse events (all) assessed by CTCAE v4.0 |
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.
Papers14
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/NCT03362047
GET https://conductscience.org/api/trials/v1/NCT03362047/registered