The Effect Of Lisinopril On Polycythemia

Part of paid clinical trials in Rochester, Minnesota.

Sponsor
Mayo Clinic
Study ID
NCT07594535
Phase
PHASE4
Status
Not Yet Recruiting

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Conditions

  • Polycythemia

Eligibility Criteria

Sex
ALL
Age
18 Years - 80 Years
Healthy Volunteers
Not accepted

Interventions

  • Lisinopril Tablets — DRUG
    Subjects will be treated with Lisinopril in three phases: Phase 1: Baseline-3 weeks: 2.5 mg dose Phase 2: Weeks 4 - 7: 5 mg dose (2 x 2.5mg tablets) Phase 3: Weeks 8-12: 10 mg dose (4 x 2.5 mg tablets)

Study Details

The purpose of this study is to evaluate the effect of the (angiotensin-converting enzyme) ACE inhibitor lisinopril on hemoglobin, hematocrit, and erythropoietin levels in patients with secondary polycythemia due to high-oxygen-affinity hemoglobin variants, oxygen-sensing pathway mutations, or other unexplained and potentially irreversible forms of erythrocytosis. This study aims to determine whether ACE inhibition can effectively reduce excessive erythrocytosis by modulating erythropoietin production.

Key Dates

Start date
Jul 1, 2026
Status verified
May 2026
Primary completion
Jul 1, 2028
Completion
Jul 1, 2029

Study Design

Enrollment
30 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: Lisinopril
    Patients diagnosed with polycythemia will be treated with Lisinopril, 2.5 mg tablets

Primary Outcome Measure

Change in hemoglobin [ Time Frame: Baseline (dose 0), study day 3 (dose 2.5), study day 5 (dose 5.0), and study day 7 (dose 10.0) ]

Central Contacts

  • Nancy Meyer
    507-255-0913

Locations (1)

FacilityCityStateZIPSite coordinators
St. Mary's HospitalRochesterMinnesota55902-

Find similar trials in Rochester, MN

By research site
St. Mary's Hospital· Rochester, MN

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