Multihormonal Deficiencies and miRNA Profile in Chronic Heart Failure: Effects of Combined Hormonal Replacement Therapy

Sponsor
IRCCS SYNLAB SDN (Other)
Overall Status
Completed
CT.gov ID
NCT05769387
Collaborator
(none)
250
1
48
5.2

Study Details

Study Description

Brief Summary

The results from this study will be useful to gain detailed information on the correlation related to pathophysiological aspects between endocrine system and clinical status of patients with heart failure, and to identify factors correlated with the progression and prognosis of ICC

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    250 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Multihormonal Deficiencies and miRNA Profile in Chronic Heart Failure: Effects of Combined Hormonal Replacement Therapy
    Actual Study Start Date :
    May 23, 2018
    Actual Primary Completion Date :
    Jan 31, 2020
    Actual Study Completion Date :
    May 22, 2022

    Arms and Interventions

    Arm Intervention/Treatment
    Patients with no hormonal deficit

    Patients with hormonal deficiencies

    Outcome Measures

    Primary Outcome Measures

    1. Evaluation of the association between hormonal deficits (single or multiple), miRNA profile and clinical/functional indices in patients with heart failure [1-48 months]

      Patients will be followed with the goal of determining whether the deficits hormonal deficits have an impact on prognosis. In the pilot study, a significant benefit is expected in terms of improved quality of life and physical performance of patients following adequate hormone replacement treatment. In addition, the clinical relevance of the association between anabolic deficits (single or multiple), miRNA expression profile, vitamin D levels, and clinical/functional indices in patients with HCI in order to identify novel biomarkers for the progression of human collagenase inhibitor HCI

    2. Evaluation of clinical and morphological effects where necessary in patients With multiple hormonal deficits in addition to standard medical therapy [1-48 months]

      Evaluation of the prognostic impact of hormone deficits and miRNA levels in a large population of heart failure patients

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • ischemic or idiopathic dilated cardiomyopathy, stable medications for at least three months including ß-blocker that must be started at least 6 months before entering the study, fraction of left ventricular ejection less than or equal to 49%
    Exclusion Criteria:
    • Age < 18 years, Inability to perform a bicycle ergometer exercise test. Diabetes mellitus in poor glycometabolic control and/or proliferative retinopathy or nonproliferative retinopathy severe grade. Severe renal failure; Hepatic cirrhosis advanced. Active neoplastic disease or history of malignancy. Patients with severe acute illness caused by complications from open heart or abdominal surgery, multiple accidental trauma, or acute respiratory failure. Active infection or sepsis. Any allergies to growth hormone, testosterone, vitamin D, or other excipients such as benzyl alcohol, sucrose, phosphoric acid, sodium hydroxide, or methacresol. Acute Coronary Syndrome within the previous 6 months

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 IRCCS Synlab SDN Naples Italy 80143

    Sponsors and Collaborators

    • IRCCS SYNLAB SDN

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    IRCCS SYNLAB SDN
    ClinicalTrials.gov Identifier:
    NCT05769387
    Other Study ID Numbers:
    • 5-18
    First Posted:
    Mar 15, 2023
    Last Update Posted:
    Mar 15, 2023
    Last Verified:
    Mar 1, 2023
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 15, 2023