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Iron infusion trial aims to boost exercise in lung disease patients

NCT ID NCT07359599

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether giving iron through a vein can help people with pulmonary hypertension (high blood pressure in the lungs) who also have low iron levels. Many patients with this condition have trouble absorbing iron from pills. The trial will compare intravenous iron to a placebo in 306 participants, measuring how far they can walk in six minutes and their quality of life after 24 weeks.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
ferric carboxymaltose (intravenous iron)
What this could lead to
If it works, this could offer a new way to improve exercise capacity and quality of life for many pulmonary hypertension patients who also have iron deficiency.
What could go wrong
This is a phase 4 trial, but it's still uncertain whether correcting iron deficiency will actually improve symptoms. The study is relatively small and the effect may be modest or absent.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Phase 4

Runs after approval, following long-term safety and how well the treatment works in everyday use.

Participants

About 306 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jan 2026

Expected to finish

Oct 2028

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * ≥18 years of age * WHO functional class II - IV * Iron deficiency defined as TSAT \<21% (no more than ≥3 months old at randomization) * PH defined by echocardiography and/or right heart catheterization (RHC) according to the following WHO groups: * Group 1 PH: * Patients with a diagnosis of idiopathic PAH, hereditary PAH, drug induced PAH or PAH and associated with CTD or CHD (historical RHC available) on stable and optimized doses of PAH targeted therapies for at least 4 weeks before randomization. * Echocardiographic evidence of a high or intermediate probability for PH as per 2022 ESC PH guidelines. * Group 2 PH and baseline LVEF \> 50% on imaging modality within last 6 months before randomization and on stable doses of loop diuretics and HFpEF therapies for 4 weeks. Group 2 PH can be included based on echocardiography or RHC.: * Echocardiography (\<6mo before randomization): * Presence of LVH or LA-enlargement * E/e' \>15 (at rest or exercise) * TRVmax \>2.8 m/s (at rest) or mPAP/CO\>3 mHg/L/min (exercise) or echocardiographic evidence of high or intermediate probability for PH as per 2022 ESC PH guidelines. * RHC (\<6mo before randomization) * mPAP \> 20 mmHg * PCWP \> 15 mmHg at rest or PCWP/CO-slope \> 2mmHg/L/min or exercise PCWP\>25mmHg, or PCWP 13-15 mmHg with elevation ≥18mmHg after 500 cc Fluid Challenge * Group 4 PH: * Inoperable CTEPH * Persistent/recurrent CTEPH (\> 1 year after endarterectomy or \> 6 months after balloon pulmonary angioplasty) ineligible for balloon pulmonary angioplasty. * Echocardiographic evidence of a high or intermediate probability for PH as per 2022 ESC PH guidelines. Exclusion Criteria: * Screening haemoglobin \< 8 g/dl or \>15 g/dl * Ferritin \> 700 ng/mL * Known hypersensitivity reaction to any component of FCM * Group 1 PH associated with veno-occlusive diseases. * Primary diagnosis of group 3 PH * Primary diagnosis of group 5 PH * Treatment with oral or other IV iron therapies at screening. * Current or planned mechanical circulatory support or lung/heart transplantation. * Any planned surgery or procedure leading to expected significant blood loss (defined as more than 250 ml = equal to 125mg of iron). * Haemodialysis or peritoneal dialysis (current or planned within the next 24 weeks). * Inability to return for follow up visits within the necessary windows * Concurrently in a study with another investigational product. * Uncorrected moderate to severe aortic stenosis (AVA \<1.5cm² and mean gradient \>20 mmHg) or severe valvular regurgitation (except tricuspid regurgitation) * Impression by investigator that patient cannot perform a 6MWT * Active infection as judged by the investigator. * Pregnancy or desire to become pregnant during the study duration.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The study's own enquiry address

    This study publishes an address for enquiries. See it below .

  2. The places running it

    7 sites. The list below names each one and where it is.

  3. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  4. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • AZ Groeninge

    NOT_YET_RECRUITING

    Kortrijk, 8500, Belgium

    Contact Email: •••••@•••••

  • AZORG

    NOT_YET_RECRUITING

    Aalst, 9300, Belgium

  • CHU Charleroi-Chimay

    NOT_YET_RECRUITING

    Lodelinsart, 6042, Belgium

  • CHU UCL Namur

    NOT_YET_RECRUITING

    Yvoir, 5530, Belgium

  • Hôpital Erasme

    NOT_YET_RECRUITING

    Brussels, 1070, Belgium

  • UZ Leuven

    NOT_YET_RECRUITING

    Leuven, 3000, Belgium

  • Ziekenhuis Oost-Limburg

    RECRUITING

    Genk, 3600, Belgium

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