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Persistent Pulmonary Hypertension After Percutaneous Mitral Commissurotomy

Predictors of Persistent Pulmonary Hypertension After Percutaneous Mitral Commissurotomy and Its Impact on Clinical Outcomes

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04083729
Enrollment
62
Registered
2019-09-10
Start date
2019-09-30
Completion date
2021-10-31
Last updated
2019-09-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pulmonary Hypertension

Brief summary

To identify clinical, echocardiographic, and hemodynamic parameters which can predict persistent PH after PMC, and also to determine the impact of persistent PH on the clinical outcomes.

Detailed description

Pure mitral Stenosis develops in approximately 40% of all patients with rheumatic heart disease, and is frequently complicated by Pulmonary hypertension (PH). Pulmonary hypertension influences symptomatology and long-term prognosis. Percutaneous Mitral Commissurotomy (PMC), was first described in 1984, has good results and is performed by antegrade access to the mitral valve through trans-septal puncture by one of various techniques (e.g. Inuoe, and multitrack system). Pulmonary artery pressures (PAP) decrease following PMC. The improvement in pulmonary hypertension after PMC is explained by the improvement in the mitral valve area and subsequent decompression of left atrium (LA) and pulmonary venous beds. Even though there have been studies showing excellent results following PMC in all grades of PH, nonregression of PH following PMC is not uncommon. The component of PAP contributed by the passive transmission of the elevated LA pressure regresses immediately after a successful PMC proportional to the reduction in transmitral gradient. The PH contributed by pulmonary arteriolar constriction slowly comes down over weeks or a few months, But a fixed component due to pulmonary vascular disease usually persists.

Interventions

Percutaneous mitral commissurotomy is performed by experienced interventional cardiologists using the Inoue balloon or multitrack technique. During the procedure, conventional hemodynamic parameters are monitored. A successful immediate result is defined as a mitral valve area \> 1.5 square cm with less than moderate to severe mitral regurgitation.

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

percutaneous mitral commissurotomy

Intervention model description

predictors of Persistent Pulmonary Hypertension After Percutaneous Mitral Commissurotomy

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Severe mitral stenosis (mitral valve area ≤1.5cm). * Significant dyspnea. * Favorable anatomical characteristics for PMC as assessed by transthoracic echocardiography

Exclusion criteria

* Significant mitral regurgitation (≥ grade II/IV). Bilateral commissural calcification. * Presence of other lesions which need open heart surgery. * Wilkins' score \> 12. * Persistent LA thrombus despite adequate anticoagulation. * End stage renal or liver disease. * Patients with severe COPD and other chest problems that might be complicated by pulmonary hypertension per se.

Design outcomes

Primary

MeasureTime frameDescription
Composite of cardiovascular eventParticipants will be followed for a minimum follow-up of one monthComposite of cardiovascular mortality, cerebral infarction, systemic embolic events ,RV failure ,MV re stenosis that occurred during follow-up, and PMC-related complications; procedural mortality and urgent MV surgery. parameters changes from base line study and after follow up as MVA in cm 2,PASP in mmHg,LAP in mmHg,LVEP in mmHg,PVR in wood unit

Contacts

Primary ContactMohamed abdelfatah Ahmed
drmohamedabdelfatah@yahoo.com+2001121560152
Backup ContactAmr Elbadry ibrahim
aelbadry@aun.edu.eg+2001060701601

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026