ClinicalTrials.Veeva

Menu

Cardiac Arrhythmias at Extreme Altitude (SUMMIT)

I

Insel Gruppe AG, University Hospital Bern

Status

Enrolling

Conditions

Bradycardia
Tachycardia, Supraventricular
Arrhythmias, Cardiac
Tachycardia, Ventricular

Treatments

Diagnostic Test: Ambulatory rhythm recording

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Background: Exposure to high altitudes has been associated with an increased risk of cardiac arrhythmias in healthy subjects and an increased risk of sudden cardiac death.

Aim: The aim of the present study is to evaluate the risk and the incidence of cardiac arrhythmias at extreme altitude.

Methods: This is a prospective cohort study of healthy volunteers determined to climb Mount Everest. Subjects will be evaluated for eligibility by electrocardiography and echocardiography. All study participants will undergo ambulatory rhythm monitoring in their home environment within 12 weeks of the climb. Subsequently, ambulatory rhythm monitoring will be repeated during the ascent from basecamp to the summit of Mount Everest. The primary endpoint will be the composite of supraventricular and ventricular tachyarrhythmias, and bradyarrhythmias.

Full description

Background: Several physiological changes at high altitude give rise to a pro-arrhythmic milieu. A fall in atmospheric pressure at high altitude decreases the partial pressure of oxygen (PaO2) and causes arterial hypoxemia. Respiratory alkalosis secondary to hyperventilation causes hypokalemia and hypocalcemia. Both factors facilitate the occurrence of rhythm disturbances, and may be further exacerbated in an adrenergic state with increased epinephrin levels.

Objectives: The primary objective is to investigate the incidence of supraventricular and ventricular tachyarrhythmias, and the incidence of bradyarrhythmias in climbers during the ascent of Mount Everest. The secondary objective is to investigate clinical, electrocardiographic and echocardiographic predictors of cardiac arrhythmias at extreme altitude.

Methods: This is a prospective cohort study of healthy volunteers climbing Mount Everest. Subjects will be evaluated for eligibility by electrocardiography and echocardiography. All participants will undergo a stress test in order to rule out pre-existing rhythm disturbances during exercise. Study participants will undergo ambulatory rhythm monitoring in their home environment within 12 weeks of the climb. Subsequently, subjects will repeat ambulatory rhythm monitoring during the ascent from basecamp to the summit of Mount Everest. The subjects will act as their own controls.

Enrollment

30 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age ≥18 years
  • Normal electrocardiogram
  • Normal echocardiography
  • Written informed consent

Exclusion criteria

  • Known cardiac arrhythmia
  • Evidence of AV-block, left bundle branch block, or repolarization disorders on electrocardiogram
  • Evidence of structural heart disease (valve disease more than mild) or compromised left ventricular ejection fraction as assessed by echocardiography
  • Symptoms or history of skin cancer, rash, skin disease, keloid or injury
  • Cardiac pacemakers, cardiac defibrillators, implantable electrical devices
  • Pregnancy, breastfeeding

Trial design

30 participants in 1 patient group

Ambulatory rhythm monitoring
Description:
Ambulatory rhythm monitoring by use of patch-type device.
Treatment:
Diagnostic Test: Ambulatory rhythm recording

Trial contacts and locations

1

Loading...

Central trial contact

Laura Morf, PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems