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The effect of acetazolamide on cognitive function in hypoxia

Phase 3
Recruiting
Conditions
ormobaric hypoxia.
Registration Number
IRCT20170326033146N5
Lead Sponsor
Razi University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Male
Target Recruitment
14
Inclusion Criteria

Male student of Razi University
Age 18 to 29 years old
BMI: 18.5 - 29.4

Exclusion Criteria

Permanent residence at altitudes above 2000 meters
History of cognitive disorders or neurological diseases
Having a chronic illness
Smoking
History of living at altitudes of more than 2000 meters in the two months before the start of a research

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Simple visual reaction time. Timepoint: The beginning of the study to assess the level of cognitive function after taking acetazolamide or placebo and after hypoxia. Method of measurement: Cognitive function is assessed using a reaction time device. ( RESPONSE PANEL63035A, LAFAYETTE, INDIANA ).;Simple auditory reaction time. Timepoint: The beginning of the study to assess the level of cognitive function after taking acetazolamide or placebo and after hypoxia. Method of measurement: Cognitive function is assessed using a reaction time device. ( RESPONSE PANEL63035A, LAFAYETTE, INDIANA ).;Selective visual reaction time. Timepoint: The beginning of the study to assess the level of cognitive function after taking acetazolamide or placebo and after hypoxia. Method of measurement: Cognitive function is assessed using a reaction time device. ( RESPONSE PANEL63035A, LAFAYETTE, INDIANA ).
Secondary Outcome Measures
NameTimeMethod
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