NCT03536455

Brief Summary

Randomized, placebo controlled trial evaluating the effect of acetazolamide on maximal exercise performance in lowlanders older than 40 years travelling from 760 m to 3'100 m.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
92

participants targeted

Target at P50-P75 for phase_4

Timeline
Completed

Started May 2018

Shorter than P25 for phase_4

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 14, 2018

Completed
1 day until next milestone

Study Start

First participant enrolled

May 15, 2018

Completed
9 days until next milestone

First Posted

Study publicly available on registry

May 24, 2018

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 2, 2018

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 2, 2018

Completed
Last Updated

October 12, 2021

Status Verified

October 1, 2021

Enrollment Period

3 months

First QC Date

May 14, 2018

Last Update Submit

October 10, 2021

Conditions

Keywords

healthy participants older than 40 yearsexercise performancepreventionacetazolamide

Outcome Measures

Primary Outcomes (1)

  • Change in maximal power output during exercise

    Difference in altitude-induced change in maximal power output between acetazolamide and placebo group.

    Day 1 at 760m and day 1 at 3'100m

Secondary Outcomes (4)

  • Change in peak oxygen uptake during exercise

    Day 1 at 760m and day 1 at 3'100m

  • Change in cerebral tissue oxygenation during exercise

    Day 1 at 760m and day 1 at 3'100m

  • Change in muscle tissue oxygenation during exercise

    Day 1 at 760m and day 1 at 3'100m

  • Change in arterial blood gasses at rest and peak exercise

    Day 1 at 760m and day 1 at 3'100m

Study Arms (2)

ACETAZOLAMIDE oral capsule

ACTIVE COMPARATOR

Acetazolamide 375mg/day (capsule @125 mg: 1 in the morning, 2 in the evening), orally. Medication starts 24 hours before ascent to 3'100m until the morning after the second night at 3'100m

Drug: ACETAZOLAMIDE oral capsule

PLACEBO oral capsule

PLACEBO COMPARATOR

Placebo (capsules identically looking as acetazolamide capsules: 1 in the morning, 2 in the evening), orally. Medication starts 24 hours before ascent to 3'100m until the morning after the second night at 3'100m

Drug: Placebo oral capsule

Interventions

Administration of 1x125mg acetazolamide in the morning, 2x125mg in the evening, starting 24 hours before departure to 3'100m

ACETAZOLAMIDE oral capsule

Administration of equally looking placebo capsules in the morning and evening, starting 24 hours before departure to 3'100m

PLACEBO oral capsule

Eligibility Criteria

Age40 Years - 75 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Healthy men and women, age 40-75 yrs, without any disease and need of medication.
  • Born, raised and currently living at low altitude (\<800m).
  • Written informed consent.
  • Kyrgyz ethnicity

You may not qualify if:

  • Any active respiratory, cardiovascular or other disease requiring regular treatment or being otherwise relevant for tolerance of hypoxia or altitude exposure.
  • Any condition that may interfere with protocol compliance including current heavy smoking (\>20 cigarettes per day or \>20 pack-years with active smoking during the last 10 years), regular use of alcohol.
  • Allergy to acetazolamide and other sulfonamides.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

National Center of Cardiology and Internal Medicine

Bishkek, 720040, Kyrgyzstan

Location

MeSH Terms

Conditions

Altitude Sickness

Interventions

Acetazolamide

Condition Hierarchy (Ancestors)

Respiration DisordersRespiratory Tract Diseases

Intervention Hierarchy (Ancestors)

ThiadiazolesThiazolesSulfur CompoundsOrganic ChemicalsAzolesHeterocyclic Compounds, 1-RingHeterocyclic Compounds

Study Officials

  • Konrad E Bloch, MD

    University Hospital, Zürich

    STUDY CHAIR
  • Talant M Sooronbaev, MD

    National Center of Cardiology and Internal Medicine, Bishkek, Kyrgyzstan

    STUDY DIRECTOR
  • Michael Furian, MSc

    University Hospital, Zürich

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
phase 4
Allocation
RANDOMIZED
Masking
QUADRUPLE
Who Masked
PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 14, 2018

First Posted

May 24, 2018

Study Start

May 15, 2018

Primary Completion

August 2, 2018

Study Completion

August 2, 2018

Last Updated

October 12, 2021

Record last verified: 2021-10

Locations