ClinicalTrials.Veeva

Menu

Colchicine for the Treatment of Cardiac Injury in Hospitalized Patients With COVID-19 (COLHEART-19) (Colheart-19)

Baptist Health South Florida logo

Baptist Health South Florida

Status and phase

Terminated
Phase 2
Phase 1

Conditions

Covid19

Treatments

Drug: Colchicine

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

This is an open-label unblinded, randomized study to treat hospitalized covid-19 patients with colchicine plus current care (per institution treating physicians) vs. current care per institution treating physicians alone (the control arm)

Full description

We aim to determine if Colchicine improves short-term outcomes in hospitalized coronavirus disease-19 (COVID-19) patients with cardiac manifestations of disease.

Myocardial injury has been described in up to 30% of COVID-19 infected patients, and portends a poor prognosis with currently no known treatment. Colchicine is a widely available, well-established, inexpensive, oral anti-inflammatory agent that has been FDA approved for the treatment of inflammatory disorders including gout and familial Mediterranean Fever. Trials have also shown its benefit to prevent post-cardiotomy syndrome, to treat acute and recurrent pericarditis, and reduce cardiovascular events after myocardial infarction. We extrapolate based on these indications and studies that colchicine may also help improve outcomes in hospitalized COVID-19 patients with evidence of cardiac injury.

This is an unblinded randomized study to treat hospitalized covid-19 patients with colchicine plus current care per institution treating physicians vs. current care per institution treating physicians alone (the control arm)

Enrollment

2 patients

Sex

All

Ages

18 to 99 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Men and Women ≥ 18 years of age

  • Covid-19 Positive

  • Hospitalized patients able to provide informed consent

  • Cardiac injury (as evidenced by any of the following)

    1. Elevated troponin level
    2. Elevated BNP level
    3. New ischemic or arrhythmogenic ECG/telemetry changes
    4. New decrease in Left Ventricular Ejection Fraction (LVEF) or new pericardial effusion on echocardiogram

Exclusion criteria

  • Pregnancy, breastfeeding mothers, and women of childbearing age who are unable to use adequate contraception, which includes:

    1. Intrauterine devices (IUD), contraceptive implants, or tubal sterilization
    2. Hormone method with a barrier method
    3. Two barrier methods
    4. If a partner's vasectomy is the chosen method of contraception, a hormone or barrier method must also be used in conjunction
  • History of severe hematologic or neuromuscular disorder

  • Co-administration of Cytochrome P450 3A4 (CYPA3A4) and P-glycoprotein transport inhibitor

  • Severe renal impairment with concomitant hepatic impairment

  • Concurrent use of colchicine and strong or P-glycoprotein inhibitor with renal or hepatic impairment

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

2 participants in 2 patient groups

Active
Active Comparator group
Description:
Hospitalized covid-19 patients treated with colchicine plus current care per institution treating physicians.
Treatment:
Drug: Colchicine
Control
No Intervention group
Description:
Hospitalized covid-19 patients treated with current standard of care (per institution treating physicians) alone.

Trial documents
1

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems