Sauna test aims to measure sweat loss in rare ROSAH syndrome

NCT ID NCT07814209

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First seen Sep 10, 2026 · Last updated Sep 11, 2026 · Updated 1 time

Summary

Researchers are testing a new way to measure how much sweat the body produces during controlled heat exposure. About 20 healthy volunteers and up to 10 people with ROSAH syndrome, a rare genetic condition that can cause reduced sweating, will sit in a temperature-controlled sauna chamber for 30 minutes. Filter papers placed on the skin before and after exposure are weighed to calculate sweat mass at several body sites. Each participant completes three sessions, and a questionnaire asks about the impact of reduced sweating.

What this could mean

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

Active substance
Standardized controlled heat exposure with gravimetric sweat collection
What this could lead to
If the method works, doctors could use it to measure sweat loss more reliably in people with ROSAH syndrome and other conditions that reduce sweating.
What could go wrong
The study is small and tests a measurement technique, not a treatment. The method may not give consistent results across people or may not work well outside the research setting.

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Study facts

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

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 30 people

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

Expected to start

Aug 2026

An estimate. Start dates often move.

Expected to finish

Dec 2027

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

12 to 18 years

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: * Male or female participants 12 to 65 years of age at screening. * Adolescent participants must be Tanner stage IV or V or have reached an equivalent level of sexual maturity. * For the healthy-volunteer cohort, the participant must be considered healthy based on medical history and investigator assessment. * For the ROSAH syndrome cohort, the participant must have a genetically and clinically confirmed diagnosis of ROSAH syndrome and must be considered clinically stable by the investigator. * Able and willing to complete three controlled sauna heat-exposure tests. * Able to remain seated in a temperature-controlled sauna chamber for up to 30 minutes. * Willing to wear only underwear during testing; female participants may wear a bra. * Willing to have hair at testing sites trimmed or shaved if necessary. * Able to drink 300 mL of water before each test. * Able and willing to comply with study requirements, instructions, and protocol restrictions and likely to complete the study as planned. * Able to provide written informed consent. * For minors, written informed consent must be provided by a parent or legal representative, and written assent must be provided by the participant. Exclusion Criteria: * Baseline body temperature greater than 37.5°C on the day of testing. * Fever, acute infection, or acute illness within 7 days before testing. * History of heat stroke, severe heat intolerance, heat-associated syncope, or severe dehydration. * Clinically significant cardiovascular disease, uncontrolled hypertension, cardiac arrhythmia, or unstable respiratory disease. * Severe anemia or unstable cytopenia, in the investigator's judgment. * Active skin disease, wound, dermatitis, or skin infection at a filter paper placement site. * Pregnant or breastfeeding. * Current use of medication that may substantially affect sweating or thermoregulation unless approved by the investigator, including anticholinergic agents, systemic beta blockers, diuretics, selected antihistamines, or medications that reduce heat tolerance. * Use of depilatory cream, waxing, an epilator, or another chemical or mechanical hair-removal method other than shaving from 7 days before the first sweat test through the final sweat test. * Laser, intense pulsed light, or other energy-based hair removal within 3 months before screening. * Unable to comply with clothing, privacy, or testing requirements. * Any other condition that, in the investigator's judgment, would create an unacceptable risk or interfere with interpretation of the study results.

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Conditions

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As listed by the trial registrant

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