I.R.C.C.S. Policlinico San Donato
San Donato Milanese, Milano, 20097, Italy
Location status: Recruiting
Location contact
Antonio Popolo Rubbio, MD
PRINCIPAL_INVESTIGATOR
Federica Rossi
CONTACT
Francesco Bedogni, MD
SUB_INVESTIGATOR
NCT Number: NCT05455489
The aim of the GISE study is to confirm the MitraClip safety and improve the device effectiveness in a selected all comers ("more-comers") population with symptomatic severe mitral regurgitation undergoing/undergone Transcatheter Edge-to-Edge Repair (TEER) with MitraClip G4.
Interested in participating?
Request Info18 year and older
All sexes
Observational
San Donato Milanese, Milano, 20097, Italy
Location status: Recruiting
Antonio Popolo Rubbio, MD
PRINCIPAL_INVESTIGATOR
Federica Rossi
CONTACT
Francesco Bedogni, MD
SUB_INVESTIGATOR
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
SUBGROUP A: FUNCTIONAL MR Patients with symptomatic severe secondary MR (3-4+, according to the multiparametric study algorithm), both ischemic or non-ischemic etiology, on optimal medical therapy AND
THE MULTIPARAMETRIC ALGORITHM FOR MR GRADING The multiparametric algorithm, adapted from the criteria recommended by the American Society of Echocardiography 2003 Guidelines and based on 3 tiers of evaluation, will be used for qualification purposes to determine if MR was 3+ or higher. The 3 tiers of evaluation are applied in a hierarchical manner (from tier 1 to 3) and patients qualified for TEER by meeting the criteria of at least one of them. For MR grading purposes, MR severity was subsequently graded as 3+ or 4+ based on the integrative evaluation of multiple parameters recommended by the The American Society of Echocardiography (ASE)
Exclusion criteria
Time frame: at 30 days
grade ≤1+. Two separates subgroups will be identified according to the presence of functional (FMR) or degenerative (DMR) mitral valve disease.
Time frame: at 1 year
grade ≤1+. Two separates subgroups will be identified according to the presence of functional (FMR) or degenerative (DMR) mitral valve disease.
Time frame: at 30 days
all-cause death, cardiovascular death and non-cardiovascular death, myocardial infarction, hospitalizations for HF,
Time frame: at 1 year
all-cause death, cardiovascular death and non-cardiovascular death, myocardial infarction, hospitalizations for HF,
Time frame: at 2 years
all-cause death, cardiovascular death and non-cardiovascular death, myocardial infarction, hospitalizations for HF,
Time frame: at 3 years
all-cause death, cardiovascular death and non-cardiovascular death, myocardial infarction, hospitalizations for HF,
Time frame: at 4 years
all-cause death, cardiovascular death and non-cardiovascular death, myocardial infarction, hospitalizations for HF,
Time frame: at 5 years
all-cause death, cardiovascular death and non-cardiovascular death, myocardial infarction, hospitalizations for HF,
Fondazione GISE Onlus
Other
The GIOTTO4 Study: GISE Registry of Transcatheter Treatment of Mitral Valve Regurgitation With the MitraClip G4
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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