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A prospective, randomized trial of coagulant state in perioperative period with or without Huisheng oral liquid in patients with lung cancer

A prospective, randomized trial of coagulant state in perioperative period with or without Huisheng oral liquid in patients with lung cancer

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-13003325
Enrollment
Unknown
Registered
2013-06-14
Start date
2013-11-01
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

Tumor

Interventions

trial group:Take Huisheng oral liquid in perioperative period
control group:Without any anticoagulant therapy in perioperative period

Sponsors

The forth hospital of Hebei Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 69 Years

Inclusion criteria

Inclusion criteria: 1. Satisfy the primary lung cancer diagnostic criteria; 2. Have the surgical indications; 3. Aged 18~69 years, all genders; 4. The score of ECOG 0~2; 5. Expected lifetime >=3 months; 6. No components allergies; 7. No DVT, PE, stroke, AMI histories; 8. No acute spinal cord injury, joint replacement and multiple trauma of hip joint, pelvis or lower limb fracture in 1 month.

Exclusion criteria

Exclusion criteria: 1. Unsatisfy the primary lung cancer diagnostic criteria; 2. No surgical indications; 3. Allergy sufferer, or used to have severe allergic reactions; 4. Have DVT, PE, stroke, AMI histories; 5. Have acute spinal cord injury, joint replacement and multiple trauma of hip joint, pelvis or lower limb fracture in 1 month; 6. Have uncontrolled nerve or mental diseases; Poor compliance or unable to communicate; Have primary brain tumor or central neurocytoma; 7. Participate other clinical trials; 8. Have other situations that unsuitable for this trial.

Design outcomes

Primary

MeasureTime frame
Blood routine test;PT;APTT;TT;FIB;D-Dimer;AT-III;Protein-C;

Secondary

MeasureTime frame
routine urine test;liver function test;kidney function test;

Countries

China

Contacts

Public ContactGuo Yang
guoyang20010099@sina.com+86 13313311822

Outcome results

None listed

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