NCT02760186

Brief Summary

Prospective interventional trial in lowlanders evaluating effect of acute exposure, acclimatization and re-exposure to high altitude.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
21

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Mar 2016

Shorter than P25 for not_applicable

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

Study Start

First participant enrolled

March 1, 2016

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

April 12, 2016

Completed
21 days until next milestone

First Posted

Study publicly available on registry

May 3, 2016

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2016

Completed
Last Updated

May 5, 2017

Status Verified

May 1, 2017

Enrollment Period

9 months

First QC Date

April 12, 2016

Last Update Submit

May 4, 2017

Conditions

Effect of High Altitude

Outcome Measures

Primary Outcomes (1)

  • ultrasound lung comets

    change from lowland baseline at 520m, day 2 and first sojourn at 5050 m, day 2

Secondary Outcomes (1)

  • ultrasound lung comets

    first sojourn at 5050 m, 7; second sojourn at 5050m, day 2, 7

Study Arms (1)

Altitude Exposure

EXPERIMENTAL

Acute high altitude exposure followed by 7 day acclimatization and reexposure after 7 days at low altitude

Procedure: Altitude Exposure

Interventions

Altitude ExposurePROCEDURE

Altitude Exposure

Altitude Exposure

Eligibility Criteria

Age18 Years - 75 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Born, raised and currently living \<800m
  • No overnight stay at altitudes \> 1500m 4 weeks before the study

You may not qualify if:

  • Previous altitude intolerance to altitude \<3000m
  • Pregnancy
  • Health impairment, which requires regular treatment

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Switzerland

Zurich, 8091, Switzerland

Location

Study Officials

  • Konrad E Bloch, MD

    University of Zurich

    STUDY CHAIR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
PREVENTION
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

April 12, 2016

First Posted

May 3, 2016

Study Start

March 1, 2016

Primary Completion

December 1, 2016

Study Completion

December 1, 2016

Last Updated

May 5, 2017

Record last verified: 2017-05

Locations

CH(1)