ClinicalTrials.gg
RecruitingNCT07594535Updated Aug 21, 2026

The Effect Of Lisinopril On Polycythemia

A Phase 4 interventional study of Lisinopril Tablets in Polycythemia, sponsored by Mayo Clinic. Recruiting at 2 sites in United States. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2026-08-21.

Sponsored by Mayo Clinic · Phase 4, Interventional, and Treatment

From the registry’s dates

  • Started Jul 2026; still recruiting 4 months later.
Phase
Phase 4
Study type
Interventional
Enrollment
30
Allocation
Not applicable
Ages
18 Years to 80 Years
Sex
All
01

Study summary

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.

Read the detailed description

Demonstrating that ACE inhibitor therapy with lisinopril lowers hemoglobin, hematocrit, and erythropoietin levels could introduce a novel therapeutic approach for the management of secondary polycythemia due to high-oxygen-affinity hemoglobin variants, oxygen-sensing pathway mutations, or other unexplained and potentially irreversible forms of erythrocytosis, potentially reducing reliance on repeated phlebotomies and lowering thrombotic risk.

02

Conditions studied

  • Polycythemia

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03

In context

Polycythemia

32 studies on the registry are indexed under Polycythemia; 12 are open to participants now.

This study's planned enrollment of 30 is below the median of 67 across 22 interventional studies indexed under Polycythemia.

Browse Polycythemia studies →

Lead sponsor

Mayo Clinic is the lead sponsor of 3,269 studies on the registry; 672 are open to participants now.

Of its 452 completed or terminated interventional studies of FDA-regulated products, 321 (71%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • in Men: >16.5 g/dL (10.3 mmol/L).
  • Hemoglobin in Women >16.0 g/dL (10.0 mmol/L).
  • 18-40 kg/m2.

Exclusion criteria

Exclusion Criteria:

  • Positive JAK2 gene linked to Polycythemia Vera.
  • Current smoker or previous heavy smoker (>15 pack years) who quit less than 12 months prior to enrollment.
  • Resting SpO₂ ≤ 94% on room air.
  • Current or recent (within the past 6 months) use of testosterone or androgen supplementation.
  • Any confounding respiratory or renal disease, including diagnosed or suspected sleep apnea, or stage 3 and up of chronic kidney disease.
  • Any confounding hematologic disease that may alter level.
  • Currently treated with ACE inhibitors.
  • Currently treated with potassium-sparing diuretics.
  • Currently on SGLT2 or use within 4 weeks prior to screening.
  • Baseline systolic blood pressure ≤90 mmHg.
  • Baseline systolic blood pressure >160 mmHg or diastolic blood pressure >100 mmHg.
  • Occupational exposure associated with chronically elevated COHb (auto repair, etc.).
  • History of anaphylaxis or angioedema.
  • Pregnant or breastfeeding.
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Hemoglobin (Hb)

The protein in red blood cells that carries oxygen. A low level is anaemia, which can cause tiredness and breathlessness. Measured in g/dL or g/L (9 g/dL is 90 g/L).

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

05

Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
30 participants (estimated)

Study arms

  • Experimental
    Lisinopril

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

    Drug: Lisinopril Tablets

Interventions

  • 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)

06

What researchers measure

Primary outcomes

  1. Change in hemoglobin

    Hemoglobin measures the amount of a protein in red blood cells via blood sample and is reported in grams per deciliter (g/DL) Hemoglobin (Hb) concentration exceeding 16 g/dL in women and 16.5 g/dL in men is considered abnormal.

    Time frame: Baseline (dose 0), study day 3 (dose 2.5), study day 5 (dose 5.0), and study day 7 (dose 10.0)

  2. Change in hematocrit

    Hematocrit (Hct) is measured by determining the percentage of red blood cells (RBCs) in a blood sample. Hematocrit (Hct) ≥ 48% in women and ≥49% in men is considered elevated.

    Time frame: Baseline (dose 0), study day 3 (dose 2.5), study day 5 (dose 5.0), and study day 7 (dose 10.0)

  3. Change in erythropoietin

    Erythropoietin is measured via blood test to detect hormone levels, and is reported in milliunits per milliliter (mU/mL). A normal reference range is generally 4 to 26 mU/mL)

    Time frame: Baseline (dose 0), study day 3 (dose 2.5), study day 5 (dose 5.0), and study day 7 (dose 10.0)

07

Study locations

2 of 2 sites recruiting
  • Mayo Clinic
    Rochester, Minnesota 55902, United States
    Recruiting
  • St. Mary's Hospital
    Rochester, Minnesota 55902, United States
    Recruiting
    • Nancy Meyer · Contact507-255-0913
    • Michael Joyner, MD · Principal investigator
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Jul 2026 (actual). Primary completion is estimated for Jul 2028, 24 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
May 13, 2026
First posted
May 18, 2026
StartActual
Jul 1, 2026
Primary completionEst.
Jul 1, 2028
CompletionEst.
Jul 1, 2029
Last update
Aug 21, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 21, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07594535
Lead sponsor
Mayo Clinic
Responsible party
Michael J. Joyner, M.D. (Principal Investigator, Mayo Clinic) — Principal investigator
First posted
May 18, 2026
Start date
Jul 1, 2026
Primary completion
Jul 1, 2028 (estimated)
Completion
Jul 1, 2029 (estimated)
Last update
Aug 21, 2026

Study contacts

Nancy Meyer
Contact
meyer.nancy2@mayo.edu
507-255-0913
Michael Joyner, MD
principal investigator · Mayo Clinic

Oversight

Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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