Not medical advice. This website is not medical advice, a diagnosis, a match to a trial, or a recommendation to join a study. Listings are plain-English rewrites of public ClinicalTrials.gov records. Whether a site is still enrolling, and whether you qualify, can only be confirmed by the study team and your clinician. Source registry: ClinicalTrials.gov. Editorial rules: methodology.
RecruitingNot a traditional drug phaseinterventionalRules rewrite

Not a traditional drug phase: testing Infusion of levosimendan for LEVOSIMENDAN

A single-center pilot prospective randomly assigned compared with a dummy treatment neither you nor the study doctors know who gets the real treatment clinical trial. Study objective - to investigate the how well it works and safety of levosimendan in patients in the perioperative period following pulmonary endarterectomy for chronic thromboembolic pulmonary hypertension (CTEPH).

Official registry: https://clinicaltrials.gov/study/NCT07914933 · Meshalkin Research Institute of Pathology of Circulation · enrollment listed as 50

What this phase means

This study does not use the classic phase 1–4 drug ladder. It may be a device, a behavior program, a surgery timing study, or an early feasibility test.

Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.

What the registry says happens

If you join, the listed intervention(s) are Infusion of levosimendan, or Placebo infusion "Soluvit". The registry lists allocation as randomized. A single-center pilot prospective randomly assigned compared with a dummy treatment neither you nor the study doctors know who gets the real treatment clinical trial.

They plan to enroll about 50 people at Novosibirsk. Taking part typically means taking a study drug (or dummy pill) plus check-ins.

Official title (unrewritten)

The Effect of Levosimendan on Pulmonary Artery Pressure and Right Ventricular Function in the Perioperative Period in Patients With CTEPH After Pulmonary Thromboendarterectomy: a Single-center Pilot Prospective Randomized Placebo-controlled Double-blind Clinical Trial

Interventions: Infusion of levosimendan, Placebo infusion "Soluvit"

Primary outcome (registry wording): Mean pulmonary artery pressure (mPAP)

Who it is for (from inclusion criteria)

  • Ages 18 Years to any
  • Scheduled for pulmonary thromboendarterectomy surgery

Public study contact (from the registry)

Gleb Moroz, PhD

+79833177148

g_moroz@meshalkin.ru

Published on ClinicalTrials.gov. Contact them as a possible participant. They decide eligibility.

Sites listed on ClinicalTrials.gov

1 listed

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FAQ about this NCT record

Is NCT07914933 still recruiting?

The sponsor posted status “Recruiting” on ClinicalTrials.gov at last ingest. Sites can pause independently. Confirm with the official record and the listed contact.

What phase is NCT07914933?

Not a traditional drug phase. Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.

Can PlainTrials tell me if I qualify for NCT07914933?

No. The inclusion and exclusion lists on this page are readable extracts of the public eligibility block. Only the study team can screen you.

How to read a ClinicalTrials.gov record · Questions to ask the coordinator · Glossary