Skip to content

An interventional study of sildenafil in the treatment of the de adaptation to high altitude disease

An interventional study of sildenafil in the treatment of the de adaptation to high altitude disease

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-12002813
Enrollment
Unknown
Registered
2012-12-29
Start date
2010-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

de adaptation to high altitude disease

Interventions

1:sildenafil
2:Placebo

Sponsors

PLA Respiratory Institute of Internal Medicine, Xinqiao Hospital, The 3rd Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18~60 years; 2. Both gender; 3. Generations living in the low elevation area; 4. Adaptation to high altitude environment in a short term living (less than 1 year); 5. To be diagnosed as the de adaptation to high altitude disease after back to the low elevation area, the symptom is graded as slight, moderate, the sympotm scores at the range of 6~25; 6. Signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. Attended other trials or addministrated other study drug whithin four weeks before this study; 2. Suffered acute high altitude disease during lived in high altitude, and returned to low altitude area for treating high altitude pulmonary edema or/and brain edema; 3. With history of orginal organic diseases on heart, kidney, brain, lung; 4. With tumour; 5. With blood system diseases; 6. Brain disorder caused judgement unnormal; 7. To be backed to low elevation area due to not adoptation when shortly stay in high altitude; 8. Stay in high altitude longer than one year; 9. Suffered high altitude cardio disease and polycythemia when stay in high altitude; 10. To be with influenza, upper respiratory infection, infectious diarrhea after return back to low elevation area; 11. Drugs and / or alcohol abuse; 12. Unwilling to submit to test arrangement or automatically withdraw from the study.

Design outcomes

Primary

MeasureTime frame
mPA;

Secondary

MeasureTime frame
HR;LVEF;LVFS;Pulmonary artery diameter;Three tricuspid valve diastolic blood flow spectrum;de adaptation to high altitude disease score;CK;CK-MB;LDH;ET-1;NO;

Countries

China

Contacts

Public ContactWang Guansong
wanggs2003@163.com+86 023 68755644

Outcome results

None listed

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