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Clinical study of Buyang Huanwu Decoction Combined with anticoagulant early intervention on the prevention of post thrombosis syndrome of lower extremity deep vein

Clinical study of Buyang Huanwu Decoction Combined with anticoagulant early intervention on the prevention of post thrombosis syndrome of lower extremity deep vein

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2022000083
Enrollment
Unknown
Registered
2022-06-22
Start date
2022-09-01
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

post-thrombotic syndrome

Interventions

test group:Buyang Huanwu Decoction
test group:Oral Rivaroxaban Tablets

Sponsors

Wangjing Hospital of CACMS
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Conform to the above-mentioned diagnosis of deep vein thrombosis of lower extremities (medical history + ultrasound + laboratory examination); (2) aged between 30 and 75 years old; (3) not receiving systemic anticoagulation; (4) no serious cardiac, Patients with primary diseases or mental diseases such as brain, liver, kidney, malignant tumor and hematopoietic system; (5) Patients are suitable and willing to accept clinical trials and sign informed consent.

Exclusion criteria

Exclusion criteria: (1) Under 30 years old or older than 75 years old; (2) Those with recurrent DVT, or a definite diagnosis of PTS; (3) Those who have received or plan to receive systemic intravenous thrombolysis, catheter-based thrombolysis or incision for thrombectomy, (4) Patients with absolute contraindications to anticoagulation (subarachnoid and intracerebral hemorrhage, severe active hemorrhage, malignant hypertension, recent brain, eye, and spine surgery) or relative contraindications (active gastrointestinal bleeding, hemorrhagic constitution, recent stroke, recent major surgery); (5) pregnant and lactating women; (6) complicated with severe cardiovascular, renal, hepatic, peptic ulcer, hematopoietic system (7) Those who suffer from mental illness or other reasons for not cooperating; (8) Those who are allergic or known to be allergic to the drugs and their components used in this test.

Design outcomes

Primary

MeasureTime frame
Villalta score;Lower extremity circumference difference measurement;Color Doppler examination of lower extremity veins;

Countries

China

Contacts

Public ContactWU XIN

Wangjing Hospital of CACMS

13146172181@163.com13146172181

Outcome results

None listed

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