Clinical Investigation for the PoliaValve Aortic Heart Valve- India (NCT07123766) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Clinical Investigation for the PoliaValve Aortic Heart Valve- India
50 participantsStarted 2025-11-15
Plain-language summary
The purpose of this study is to conduct a clinical investigation of the HeartHill PoliaValve Aortic Valve to collect evidence on the device's safety and performance.
Who can participate
Age range45 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Is 45 years or older
* Provide written informed consent prior to trial procedures after standard of care studies and tests indicate that the patient needs aortic valve replacement
* Agrees to attend all follow-up assessments for up to 1 year and is willing to comply with specified follow-up evaluations for the clinical trial
* Diagnosed with severe symptomatic aortic valve stenosis and/or regurgitation
Exclusion Criteria:
* Requires multiple valve replacement / repair
* Requires emergency surgery
* Has had prior valve surgery
* Requires a surgical procedure outside of the cardiac area
* Requires a cardiac procedure other than a CABG or root enlargement or aortic root replacement
* Requires or are planning another unrelated surgery within 12 months of undergoing implantation of the study device
* Has active endocarditis/myocarditis or within 3 months to the scheduled surgery
* Has renal insufficiency as determined by creatinine (S-Cr) level as ≥ 1.5 mg/dl or end-stage renal disease requiring chronic dialysis at screening visit
* Has MRI or CT scan confirmed stroke, cerebrovascular accident (CVA) or transient ischemic attack (TIA) within 3 months (90 days) prior to planned valve surgery
* Has acute myocardial infarction (AMI) within 30 days prior to planned valve surgery
* Has life expectancy to less than 12 months
* Diagnosed with hypertrophic obstructive cardiomyopathy (HOCM), except patients who have isolated subaortic muscular hypertrophy diagnosed …
What they're measuring
1
Rate of Clinical Outcomes Events
Timeframe: 12 months following patient enrollment completion
Trial details
NCT IDNCT07123766
SponsorSuzhou Hearthill Medical Technology Co.,LTD