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Clinical study of Longchaijiangxue granules in the treatment of myeloproliferative neoplasms

Clinical study of Longchaijiangxue granules in the treatment of myeloproliferative neoplasms

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200005730
Enrollment
Unknown
Registered
2022-03-16
Start date
2022-03-11
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

myeloproliferative neoplasms

Interventions

Experimental group:Longchaijiangxue granules+Yigong Powder+Basic treatment
Control group:Yigong Powder+Basic treatment

Sponsors

Xiyuan Hospital of China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Meets WHO diagnostic criteria for PV, ET. (2) PLT < 1000 x 109/L and HCT < 60%. (3) Age above 18 years (including 18 years) and below 80 years (including 80 years), with no restriction on gender. (4) Voluntarily subjected to the trial and signed an informed consent form. (5) Not participating in other clinical studies.

Exclusion criteria

Exclusion criteria: (1) Cases that met the inclusion criteria but were not treated after inclusion. (2) Patients with no record of testing. (3) Those using prohibited drugs.

Design outcomes

Primary

MeasureTime frame
Gene detection;Routine Blood Test(WBC\RBC\PLT\HGB etc.);Coagulation items;

Countries

China

Contacts

Public ContactHu-Xiaomei
huxiaomei_2@163.com18610350593

Outcome results

None listed

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