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NCT06378632ClinicalTrials.gov

AN INTERNATIONAL, OBSERVATIONAL, BLINDED STUDY TO ASSESS THE PERFORMANCE OF THE CORDIO HEARO SYSTEM

An International Multi-center Observational, Single-arm, Blinded Study to Assess the Performance of the Cordio HearO System

قيد التجنيديقبل مشاركين الآن، وفقاً لسجل السجل.
التواصل مع هذه الدراسة

باختصار

Study Design: This is an international, multicenter, observational, non-interventional, prospective, blinded, single-arm, two-period study, to collect patient utterances that will be retrospectively analyzed to determine the sensitivity and UPNR of the HearO system.

رصديةمطلوب 500 مشارك45 موقعاً3 دول

الفئات

مسجَّلة في سجل واحد

يمكن أن تُسجَّل دراسة واحدة في عدة سجلات. نعرضها مرة واحدة ونربط بكل سجل نحتفظ به.

تُعرض معلومات التجربة كما نشرها السجل، بلغتها الأصلية.

هل أنت مهتم بهذه الدراسة؟

تسجيل الدخول أو أنشئ حسابًا لتسجيل اهتمامك ومتابعة هذه الدراسة.

How this study is set up

The points below are drawn from the public registry record for this study. Each one cites the field or sentence it came from. A dash (—) means the record does not state something — not that it is missing or wrong. Many well-run studies, especially small ones, leave some of these blank.

  • Not stated: Registered after enrolment began (about 801 days after the recorded start)First posted 2024-04-22; recorded start 2022-02-11
  • Present: Has a defined primary outcomeA primary outcome measure is listed in the record
  • Present: The primary outcome states a time frameThe primary outcome measure records a time frame
  • Not stated: Whether participants are randomly assigned is not stated in the registry recordNo allocation method is recorded
  • Not stated: Whether there is a comparison group is not stated in the registry recordThe record does not describe the study arms
  • Not stated: Whether the study is blinded is not stated in the registry recordNo masking information is recorded
  • Not stated: An ethics committee is not stated in the registry recordThis registry's ingested record has no ethics-committee field
  • Not stated: Regulatory oversight (such as an IND or IDE) is not stated in the registry recordThis registry's ingested record has no regulatory-authorisation field
  • Not stated: A data monitoring committee is not stated in the registry recordThis registry's ingested record has no data-monitoring-committee fieldA data monitoring committee is not required for many smaller studies, and its absence here is not unusual.
  • Present: No cost to participants is mentioned in the recordChecked the summary, description and eligibility text; no cost-to-participant phrase found
  • Present: Sponsor has 1 other study in this databaseCounted from the lead sponsor named in the record (Cordio Medical)
  • Not stated: No posted results from this sponsor are in this database yetBased on the sponsor’s studies in this database
  • The record lists 1 condition.
  • Lead sponsor type recorded as: industry.

Trial stature

Three independent measures of this study, described from its registry record — not a recommendation about it. A rigorous study by investigators nobody has heard of is better evidence than a weak study led by a famous one. How these are scored.

Methodological rigourEXPLORATORY

An exploratory-stage design for a study of this type, judged from its ClinicalTrials.gov record.

How this score is built
  • Randomised allocation0/20

    Allocation not stated in the record

  • Blinding0/20

    Masking not stated in the record

  • Control arm0/15

    No comparator arm stated in the record

  • Primary-outcome specificity10/10

    Named primary outcome with a defined time frame

  • Endpoint type7/10

    Clinical-event endpoint

  • Multi-centre8/8

    Multi-centre: 45 sites

  • Data monitoring committee0/7

    No data monitoring committee stated

  • Prospective registration0/5

    Registered more than 30 days after the study start

  • Protocol / SAP posted0/5

    No protocol or SAP posted to the registry

ScaleMEDIUM

A medium-sized study, international in scope: 500 participants (target), run at 45 sites, across 3 countries.

How this score is built
  • Enrolment26/40

    500 participants (target)

  • Site count19/25

    45 sites

  • Country count7/15

    3 countries

  • Planned duration8/10

    Planned over about 42 months

  • Sponsor scale1/10

    Cordio Medical has led 2 trials in our corpus

Investigator standingUNKNOWN

We have no verifiable track record for the investigator named on this trial. That is common for early-career investigators and for records held outside ClinicalTrials.gov — it is not a negative signal.

How this score is built
  • Investigator standing0/100

    No investigator recorded in the registry for this trial

These describe the registry record only, and today we hold ClinicalTrials.gov data. Absent fields lower a score, and absence often reflects registration practice rather than study quality. A high-stature trial is not necessarily safer or a better choice for you — enrolling in a large definitive trial can mean a higher chance of receiving placebo, while a small early-phase study may be the only route to a new therapy.

ملخص

Study Design: This is an international, multicenter, observational, non-interventional, prospective, blinded, single-arm, two-period study, to collect patient utterances that will be retrospectively analyzed to determine the sensitivity and UPNR of the HearO system.

Two periods: Run-In period will be a period in which patients will submit daily recordings, baseline creation Core period will be a period in which patients will be followed up and will continually submit daily recordings for up-to 24 months per patient or until End-of-Study (EOS), whichever comes first.

الحالات

  • Heart Failure

الأهلية

الأهلية
الجنسالجميع
الأعمار22 Yearsلا حد أقصى
المتطوعون الأصحّاءلا
طريقة أخذ العيناتNON_PROBABILITY_SAMPLE

مجتمع الدراسة

Outpatient clinics

الأهلية كما كُتبت في السجل

Major Inclusion Criteria: 1. Age 22 or greater 2. Diagnosed with Symptomatic Chronic Heart Failure \[NYHA II-IVa (ambulatory)\] 3. At least one of the following: 1. One ADHF hospitalization in the last 12 months 2. One unplanned IV/SC diuretic administration in the last 6 months 3. Two unplanned IV/SC diuretic administrations in the last 12 months 4. NTProBNP \>500 pg/ml 4. Clinically stable HF according to investigator discretion 5. Willing to participate as evidenced by signing the written informed consent. Major Exclusion Criteria: 1. Unable to comply with daily use of the App, 2. Has had a major cardiovascular event within 3 months prior to enrolment. 3. Had a Cardiac Resynchronization Therapy Device (CRT) implanted or upgrading ≤ 1 month prior to screening visit. 4. Has estimated Glomerular Filtration Rate (eGFR) \< 30 ml/min/1.73. 5. Is likely to undergo heart transplantation/ LVAD within 6 months of Screening Visit. 6. Was treated for a significant COPD

الأهلية في عبارات بسيطة

لم تُقسَّم معايير هذا السجل إلى عبارات منفصلة بعد. نص السجل أعلاه كامل وهو النسخة المُعتمَدة.

تصميم الدراسة

تصميم الدراسة
نوع الدراسةرصدية
المرحلةغير مذكور في سجل السجل
التخصيصغير مذكور في سجل السجل
نموذج التدخّلغير مذكور في سجل السجل
الغرض الأساسيغير مذكور في سجل السجل
التعميةغير مذكور في سجل السجل
التجنيدمطلوب 500 مشارك

الجهة الراعية والمتعاونون

  • Cordio Medical الجهة الراعية

التدخلات

  • جهاز Hearo App

    No intervention - only data collection

مقاييس النتائج

  1. مقياس النتيجة الأولي

    Heart Failure Events (HFEs)

    Until the end of the study, each participant will be assigned to one of the following event outcomes: 1. Having at least one protocol-defined Heart Failure Event (HFE) in the CORE period 2. Having no Heart Failure Event (HFE) during the entire CORE period

    الإطار الزمني EOS is defined as when a total of at least 78 first usable and CEC-adjudicated HFEs have occurred or up-to 24 months per patient

التواريخ

التواريخ
تاريخ البدء11 فبراير 2022 (فعلي)
الإتمام الأولي1 يوليو 2025 (تقديري)
الإتمام15 يوليو 2025 (تقديري)
أول نشر22 أبريل 2024 (فعلي)
آخر تحديث26 مارس 2025
النتائج منشورةغير مذكور في سجل السجل
آخر تأكيد للحالةمارس 2025

فعلي يعني أن الحدث وقع. تقديري يعني أن الجهة الراعية تتوقعه. للكلمتين معنيان مختلفان.

المواقع

45 موقعاً قيد التجنيد

Israel

Israel
المنشأةالمدينةالولاية أو المنطقةالحالة
University Hospital Samson Assuta AshdodAshdodقيد التجنيد
Assuta Be'er Sheva Medical CenterBeershebaقيد التجنيد
Rambam Medical CenterHaifaقيد التجنيد
Shaare Zedek Medical CenterJerusalemقيد التجنيد
Galiee Medical CenterNahariyaقيد التجنيد
Tel Aviv Sourasky (Ichilov) Medical CenterTel Avivقيد التجنيد
Poriya Medical CenterTiberiasقيد التجنيد

Spain

Spain
المنشأةالمدينةالولاية أو المنطقةالحالة
Hospital Universitari Germans Trias i PujolBadalonaقيد التجنيد

United States

United States
المنشأةالمدينةالولاية أو المنطقةالحالة
Mission HospitalAshevilleNorth Carolinaقيد التجنيد
West Georgia CardiologyCarrolltonGeorgiaقيد التجنيد
University of ChicagoChicagoIllinoisقيد التجنيد
Advocate Illinois Masonic Medical CenterChicagoIllinoisقيد التجنيد
The Lindner Research Center at The Christ HospitalCincinnatiOhioقيد التجنيد
Cleveland ClinicClevelandOhioقيد التجنيد
The Ohio State UniversityColumbusOhioقيد التجنيد
Nature Coast Clinical ResearchCrystal RiverFloridaقيد التجنيد
Advocate Illinois Masonic Health CenterDowners GroveIllinoisقيد التجنيد
St. Elizabeth HealthcareEdgewoodKentuckyقيد التجنيد
Eastern Shore Research InstituteFairhopeAlabamaقيد التجنيد
Moses H. Cone Memorial HospitalGreensboroNorth Carolinaقيد التجنيد
Cardiovascular Institute of the SouthHoumaLouisianaقيد التجنيد
Jacksonville Center for Clinical ResearchJacksonvilleFloridaقيد التجنيد
UC San Diego HealthLa JollaCaliforniaقيد التجنيد
Cardiovascular Institute of the SouthLafayetteLouisianaقيد التجنيد
Nebraska Heart CenterLincolnNebraskaقيد التجنيد
VA Loma Linda Healthcare SystemLoma LindaCaliforniaقيد التجنيد
Rio Grande Regional HospitalMcAllenTexasقيد التجنيد
Baptist Health (Miami Cardiac & Vascular Institute)MiamiFloridaقيد التجنيد
Advance Medical Research Services Corp (AMRS)MiamiFloridaقيد التجنيد
Amavita Clinical ResearchMiamiFloridaقيد التجنيد
Midwest Cardiovascular CenterNapervilleIllinoisقيد التجنيد
Vanderbilt University Medical CenterNashvilleTennesseeقيد التجنيد
University Medical Center New OrleansNew OrleansLouisianaقيد التجنيد
Mount Sinai MorningsideNew YorkNew Yorkقيد التجنيد
The Mount Sinai HospitalNew YorkNew Yorkقيد التجنيد
VA Southern Nevada Healthcare SystemNorth Las VegasNevadaقيد التجنيد
Comprehensive Medical & Research CenterPlantationFloridaقيد التجنيد
St. Francis HospitalRoslynNew Yorkقيد التجنيد
St. Johns Center for Clinical ResearchSaint AugustineFloridaقيد التجنيد
Methodist Hospital of San AntonioSan AntonioTexasقيد التجنيد
VA San DiegoSan DiegoCaliforniaقيد التجنيد
Kaiser Permanente San FranciscoSan FranciscoCaliforniaقيد التجنيد
University of California, San FranciscoSan FranciscoCaliforniaقيد التجنيد
Tampa General HospitalTampaFloridaقيد التجنيد
Robert J. Dole VA Medical CenterWichitaKansasقيد التجنيد

مستندات الدراسة

لا تُرتبط أي مستندات في سجل السجل هذا.

التغيّرات عبر الزمن

لم تُسجَّل أي تغييرات منذ أن أدرجنا هذا السجل لأول مرة.

يُسجَّل تغيير في كل مرة تحدّث فيها الجهة الراعية سجل السجل. تظهر هنا الحالة والتواريخ والتجنيد والمواقع كلما تغيّرت.