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Treatment trial of high altitude cough

Treatment of high altitude cough (HAC) with salmeterol 50 µg and fluticasone 250 µg, one puff twice daily (bid) on Mount Everest: a randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN76835758
Enrollment
72
Registered
2010-04-16
Start date
2010-04-01
Completion date
Unknown
Last updated
2015-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

High altitude cough (HAC) Respiratory Cough

Interventions

Please note that as of 30/07/10 this trial has been extended from 01/10/2010 to 01/10/2011 The study will take place in the Everest base camp (5300 m). Mountaineers as they ascend to base camp will

Sponsors

University of Oxford (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Healthy men or women 2. Between the ages of 18 and 65 years 3. Have HAC, defined as persistent (greater than 1 day) sometimes paroxysmal cough that disturbs sleep or daily activity or both. The cough may be dry or productive but is not associated with fever, chills, shortness of breath or desaturation less than 75% at Everest Base Camp (EBC) (5300 m).

Exclusion criteria

Exclusion criteria: 1. Individuals with other obvious diagnoses causing cough (e.g., viral or bacterial pneumonia, high altitude pulmonary oedema [HAPE]) 2. Unwillingness to comply with study treatment 3. Lack of informed consent 4. Individuals on beta agonists or steroid inhalers, steroid nasal sprays or oral steroids within the last 2 weeks

Design outcomes

Primary

MeasureTime frame
The incidence of HAC using the modified the Leicester Cough Questionnaire before and after the rotahaler intervention. Measured at day 0, day 7 and day 14 of the study.

Secondary

MeasureTime frame
Measured at day 0, day 7 and day 14 of the study: 1. Oxygen saturation 2. Peak flow 3. Pulse 4. Lung auscultation

Countries

Nepal

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026