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NCT05885425

Management of Telemedicine Monitoring of Patients With Chronic Heart Failure

Status unknown Last updated 2 June 2023
What this trial tests

trial testing Telemedicine correction of medical treatment in Congestive Heart Failure Chronic in 200 participants. Status unknown.

Timeline
1 September 2023
Primary endpoint
1 May 2024
1 September 2024

Quick facts

Lead sponsorTrnava University in Trnava
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment200
Start date1 September 2023
Primary completion1 May 2024
Estimated completion1 September 2024

Drugs / interventions tested

Conditions studied

Sponsor

Trnava University in Trnava

Who can join

Adults 45 to 75, any sex, with Congestive Heart Failure Chronic. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Objective: to evaluate the possibilities and effect of telemedicine monitoring and management of patients with CHF (compared to patients with CHF without intensive telemedicine monitoring) on quality of life, prognosis and the presence of complications and hospitalisations. Patients with a stable form of congestive heart failure will be gradually included in the study. Half of them will be defined by random selection to intervention group. Parameters, that can be measured at home will be periodically telemedical monitored. In according with at home monitored data, the own physician will be able to intervene with change of medical treatment in the case of non-physiological deviations in order to improve the health status as well as the prognosis of the patient with CHF.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Congestive Heart Failure Chronic

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05885425.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing