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Clinical study of Xuefu Zhuyu Capsule in the treatment of acute chest pain after thoracoscopic surgery for early non-small cell lung cancer

Clinical study of Xuefu Zhuyu Capsule in the treatment of acute chest pain after thoracoscopic surgery for early non-small cell lung cancer

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200005757
Enrollment
Unknown
Registered
2021-09-23
Start date
2021-09-20
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

NSCLC

Interventions

Treatment group:Xuefu zhuyu capsule
Treatment group:Routine treatment of postoperative Western Medicine

Sponsors

Peking University People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age 18-75 years old (including 18 and 75 years old); 2. Those who underwent thoracoscopic lobectomy; 3. Patients with postoperative pathological diagnosis of primary lung cancer or precancerous lesions; 4. No chest pain before operation, postoperative pain within 3 months, and NRS score = 4; 5. Those who meet the TCM diagnostic criteria of qi stagnation and blood stasis syndrome; 6. Voluntarily participate in clinical research and sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Those who meet the diagnostic criteria of primary bronchial lung cancer and have been treated with radiotherapy, chemotherapy, targeted therapy and traditional Chinese medicine in the first 3 months; 2. Have mental illness, such as unconsciousness and communication disorder; 3. Patients with serious heart, liver, kidney and cerebrovascular diseases; 4. Allergic constitution or allergic to the ingredients of Xuefu Zhuyu Capsule and various drugs; 5. Those who participated in other clinical studies within 3 months before screening; 6. Pregnant or ready for pregnancy, lactating women; 7. The researcher considers it inappropriate to participate in this study.

Design outcomes

Primary

MeasureTime frame
NRS;

Secondary

MeasureTime frame
TCM syndrome score;QLQ-C30;CRP;HAMD;HAMA;

Countries

China

Contacts

Public ContactFeng Cuiling
fengcuiling@sina.com15901341502

Outcome results

None listed

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