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Intermittent Hypoxia Intervention in MS Patients (MSHYPE)

U

Universitätsklinikum Hamburg-Eppendorf

Status

Completed

Conditions

Multiple Sclerosis

Study type

Observational

Funder types

Other

Identifiers

NCT04635033
MS HYPE Pilot

Details and patient eligibility

About

This observational cohort study investigates the safety and feasibility of an intermittent hypoxia intervention in multiple sclerosis.

Enrollment

12 patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18-60 years
  • confirmed MS (all types of MS)
  • ability to come to the outpatient clinic 2-3x/week for 3 months
  • EDSS ≤ 6.5
  • inconspicuous medical examination
  • inconspicuous ECG

Exclusion criteria

  • relapse in the last 3 months
  • EDSS progression in the last 6 months
  • pregnancy
  • contraindication for MRI
  • severe heart disease
  • severe asthma, COPD
  • cancer
  • severe cognitive deficits
  • chronic headache
  • renal insufficiency
  • anaemia (Hb < 10 g/dl)
  • insulin-dependent diabetes mellitus
  • severe vascular stenosis
  • former episodes of severe high mountain sickness
  • cancer

Trial design

12 participants in 1 patient group

Intervention
Description:
2 hours of reduced FiO2 (11-15%) in the inspired air, 2-3x/week, 3 months

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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