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Lung transplant patients aim for aconcagua summit in landmark altitude study

NCT ID NCT07479511

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 follows 30 lung transplant recipients and healthy volunteers as they prepare for and climb Mount Aconcagua (6,971 meters). Participants first use a special tent at home for eight weeks to get used to lower oxygen levels. Then, a team monitors their lung function, oxygen levels, and symptoms during the actual climb. The goal is to learn how well transplant lungs adapt to extreme altitude and whether such expeditions are safe.

What this could mean

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

Active substance
intermittent hypoxic conditioning via normobaric hypoxic tent
What this could lead to
If successful, this could show that lung transplant recipients can safely adapt to extreme altitudes, potentially improving their physical fitness and quality of life.
What could go wrong
This is a small observational study (30 participants) with no control group for the intervention. High-altitude exposure carries risks like acute mountain sickness, and results may not apply to all transplant recipients.

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.

Participants

About 30 people

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

Started

Jan 2026

Expected to finish

Jun 2026

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.

Who is studied

Lung transplant recipients and Healthy controls

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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: Lung transplant recipients: * Age ≥ 18 years * \> 1 years after lung transplantation * Stable lung function over 6 month prior to inclusion, FEV1 +/-10% from baseline * VO2peak of more than 25 ml/min/kg * Physical and mental fitness, defined as the ability to complete strenuous day trips lasting 8 to 10 hours independently without suffering from a fear of heights, an altitude exposure of at least 2500m must be confirmed. * Negative pregnancy test for women of childbearing age * Written informed consent Healthy volunteers: * Age ≥ 18 years * VO2peak of more than 25 ml/min/kg * Physical and mental fitness, defined as the ability to complete strenuous day trips lasting 8 to 10 hours independently without suffering from a fear of heights * Negative pregnancy test for women of childbearing age * Written informed consent Exclusion Criteria: Lung transplant recipients: * Age \< 18 years * Refusal to participate in the study * Pregnancy Healthy controls: * Age \< 18 years * Refusal to participate in the study * Pregnancy * Chronic obstructive pulmonary disease (COPD)

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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.

Contacts and locations

Locations

  • Medical University of Vienna

    Vienna, State of Vienna, 1090, Austria

More trials for these conditions

Other studies related to the condition(s) this trial covers.