ClinicalTrials.gg
Not yet recruitingNCT07341048ACTIVAQUpdated Jan 15, 2026

Potential Biological and Physiological Determinants for Exercice in Patients With Polycythemia Vera

An interventional study of Research samples blood viscosity and viscoelasticity: in Polycythemia and Polycythemia Vera (PV), sponsored by Hospices Civils de Lyon. Not yet recruiting at 1 site in France. Open to participants aged 18 Years to 70 Years. Per ClinicalTrials.gov, last updated 2026-01-15.

Sponsored by Hospices Civils de Lyon · Not applicable, Interventional, and Basic science

Phase
Not applicable
Study type
Interventional
Enrollment
54
Allocation
Not applicable
Ages
18 Years to 70 Years
Sex
All
01

Study summary

Polycythemia vera (PV) is a rare haematological disorder characterized by an excessive production of red blood cells, associated with the somatic JAK2 V617F mutation. Clinical manifestations are varied and often include exercise intolerance but the underlying mechanisms remain poorly understood.

Physical activity is recommended in the management of chronic diseases, but it must be tailored to the physiological profile of the patient. A cardiopulmonary exercise test (CPET) is essential to ensure safety, detect possible contraindications, and assess maximal oxygen uptake (VO₂max), a key indicator of aerobic performance.

This prospective, experimental, non-randomized study will include patients with PV followed at Lyon Sud University Hospital and for which a CPET is scheduled in their routine clinical follow-up. The primary objective is to compare VO₂max between two groups of patients: moderate (\<10%) versus marked (≥10%) extent of blood viscosity increase after the completion of the CPET. The main hypothesis is that a significant increase in blood viscosity during exercise (≥10%) is a major limiting factor in oxygen transport and leads to a reduced VO₂max, reflecting impaired exercise tolerance.

Secondary analyses will focus on hemorheological parameters, tissue oxygenation, and cardiorespiratory and metabolic responses. The study aims to better understand the biological and physiological determinants of exercise intolerance in this population.

02

Conditions studied

  • Polycythemia
  • Polycythemia Vera (PV)

Keywords

  • Blood viscosity
  • polycythemia
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 54 is below the median of 67 across 22 interventional studies indexed under Polycythemia.

Browse Polycythemia studies →

Lead sponsor

Hospices Civils de Lyon is the lead sponsor of 1,866 studies on the registry; 448 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 70 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

  • Patient aged at least 18 years and under 70.
  • Patient followed for a diagnosis of Polycytemia vera (confirmed JAK2 V617F mutation) and who were prescribed a CPET because of their wish to resume regular physical activity.
  • Patient affiliated with or benefiting from a social security scheme.

Exclusion criteria

Exclusion Criteria:

  • Any known history of heart disease or chronic respiratory illness likely to affect VO₂max independently of Polycytemia vera (e.g., asthma), according to the investigator's judgment.
  • Any known history of major thromboembolic complication, according to the investigator's judgment.
  • (BMI) greater than 35, according to the investigator's judgment.
  • Participation in another interventional research protocol that may interfere with the present study, according to the investigator's judgment.
  • Adult subject under legal protection measures (guardianship, curatorship).
  • Subject currently receiving psychiatric care.
  • Subject deprived of liberty by judicial or administrative decision.
Terms in these criteria, in plain language(1)

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.

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
Not applicable
Primary purpose
Basic science
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
54 participants (estimated)

Study arms

  • Experimental
    Polycythemia vera

    Patients diagnosed with polycythemia vera, with confirmed presence of the JAK2 V617F mutation, who wish to resume regular daily physical activity and have been prescribed an exercise test for this purpose as part of their follow-up at Lyon Sud Hospital

    Biological: Research samples blood viscosity and viscoelasticity:

Interventions

  • BiologicalResearch samples blood viscosity and viscoelasticity:

    Research samples: Blood rheology: hematocrit, blood viscosity, deformability and erythrocyte aggregation, viscoelasticity

    Also known as: the level of tissue oxygenation and hemoglobin oxygenation that will be measured by near-infrared spectroscopy (NIRS).

06

What researchers measure

Primary outcomes

  1. Blood viscosity (Centipoise) at 6 shear rates.

    Blood viscosity will be measured using a cone-plate viscometer (Brookfield, model LVDVII+ PRO, cone CPE 40) on native hematocrit blood, at 7 different shear rates: 2.25, 4.5, 11.5, 22.5, 45, 90, and 225 s-¹, using an ascending ramp shear protocol.

    Time frame: Measurements will be performed at baseline (pre-test), at 3 minutes post-CPET, and at 60 minutes post-CPET

Secondary outcomes

  1. Rheological properties of blood: deformability and aggregation of erythrocytes

    Analyses will be performed on EDTA tubes. Erythrocyte deformability will be measured by ektacytometry at 9 shear stresses (0.3-30 Pa) under isotonic conditions. Maximal elongation index (EImax) and shear stress for 50% deformation (SS₁/₂) will be recorded. Aggregation/disaggregation will be assessed by syllectometry at 40% hematocrit. Parameters include aggregation index (AI) and minimal shear rate (γmin) for full disaggregation

    Time frame: Measurements will be performed at baseline (pre-test), at 3 minutes post-CPET, and at 60 minutes post-CPET.

  2. Viscoelasticity of blood

    Viscoelastic properties of blood will be assessed using rotational thromboelastometry (ROTEM delta) on citrated blood tubes. The following tests will be performed: NATEM, TEMACT, FIBTEM, and EXTEM. For each test, the following parameters will be measured: clotting time (CT, in seconds), clot amplitude at 5, 10, 20, and 30 minutes (A5, A10, A20, A30, in mm), alpha angle (indicating clot formation velocity, in degrees), maximum clot firmness (in mm), percentage of clot lysis at 30 minutes (LI30), as well as lysis onset time (LOT) and total lysis time (LT), both expressed in seconds

    Time frame: Measurements will be performed at baseline (pre-test), at 3 minutes post-CPET, and at 60 minutes post-CPET

  3. Tissue and haemoglobin oxygenation with near-infrared spectroscopy (NIRS)

    Near-infrared spectroscopy (NIRS) will be performed using the Portamon MKIII system (Artinis) with a sampling rate of 100 Hz. This non-invasive technique involves placing surface electrodes on the skin over the vastus lateralis muscle, halfway between the anterior superior iliac spine and the patella. NIRS enables continuous monitoring of changes in oxyhemoglobin (HbO₂) and deoxyhemoglobin (HHb) concentrations, allowing for the calculation of the tissue oxygenation index (TOI)

    Time frame: Measurement will be performed during the CPET.

07

Study locations

1 site
  • Department of Sports Medicine and Physical Activity. Pulmonary Function Testing. Croix Rousse Hospital.
    Lyon, 69001, France
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 15, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07341048
Responsible party
Sponsor
First posted
Jan 14, 2026
Start date
Jan 2026 (estimated)
Primary completion
May 2027 (estimated)
Completion
May 2027 (estimated)
Last update
Jan 15, 2026

Study contacts

Emeric Stauffer, Dr
Contact
emeric.stauffer@chu-lyon.fr
+33 (0)4 72 07 18 62

Oversight

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

Not currently enrolling

This study is not yet recruiting, as verified in Jan 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion