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The Efficacy of Combination of Traditional Tibetan and Remote Ischemic Conditioning on High Altitude Polycythemia

A Randomized Controlled Trial of the Efficacy of Combining Traditional Tibetan and Remote Ischemic Conditioning on High Altitude Polycythemia

Status
UNKNOWN
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06082583
Enrollment
300
Registered
2023-10-13
Start date
2023-11-01
Completion date
2025-12-31
Last updated
2023-10-13

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

Conditions

High Altitude Polycythemia

Brief summary

A multicenter, randomized controlled trial was designed to evaluate the effectiveness and safety of the comprehensive traditional Tibetan medicine program combined with remote ischemic conditioning on high altitude polycythemia.

Interventions

DEVICERemote Ischemic Conditioning

Remote ischemic conditioning conducted by an electric auto-control device will be performed twice a day for 14 days, each session including 5-min ischemia and 5-min reperfusion.

DRUGTibetan Medicine (Shiliu Jianwei Powder, Ershiwuwei Yuganzi Pills, Qiwei Tiexue Pill)

Comprehensively Tibetan medicine for 28 days, including Shiliu Jianwei Powder, Ershiwuwei Yuganzi Pills and Qiwei Tiexue Pill, dosage of which are 1.5g daily.

Sponsors

Capital Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Patients with high-altitude polycythemia aging 18 to 65 years.

Exclusion criteria

* Allergic to Tibetan medicine ingredients; * Inappropriate to receive Tibetan medicine treatment and/or remote ischemic conditioning.

Design outcomes

Primary

MeasureTime frameDescription
The incidence of effective treatmentBaseline and 1 month after treatment.The hemoglobin levels decreased ≥20% after treatment compared to pre-treatment.

Contacts

Primary ContactYuan Wang, M.D.
wilma0106@163.com+86-135 8156 7815

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026