Status:
UNKNOWN
Efficacy Study of Comprehensive Rehabilitation Program Plus Chemotherapy in Postoperative NSCLC Patients
Lead Sponsor:
Shanghai University of Traditional Chinese Medicine
Collaborating Sponsors:
Shanghai Chest Hospital
Shanghai Pulmonary Hospital, Shanghai, China
Conditions:
Non-small Cell Lung Cancer
Eligibility:
All Genders
18-75 years
Phase:
PHASE3
Brief Summary
The investigators performed a multi-centered, randomized, placebo-controlled, prospective clinical trial on the effect of comprehensive rehabilitation program plus chemotherapy to improve quality of l...
Detailed Description
NSCLC is one of the malignancies with high incidence and mortality. In recent years, surgery become the preferred treatment for early stage of NSCLC. Patients with high risk stages IB to IIIA may unde...
Eligibility Criteria
Inclusion
- Patients with completely resected stage IB-IIIA non-small-cell lung cancer who will receive chemotherapy for the first time within 6 weeks after the operation.
- Between the ages of 18 to 75 years old;
- The score of ECOG ≥2 points
- Without major organ dysfunction: hemoglobin ≥10 g/dL, absolute neutrophil count (ANC) ≥1.5\*10\^9/L, platelets ≥100 \*10\^9/L; normal hepatic and renal function
Exclusion
- Indefinite pathological diagnosis;
- Expected survival time \< 6 months
- Combined with heart, liver, kidney and hematopoietic system and other serious diseases
- The patient was treated with antibiotics or infected one week before the test;
- Pregnant or child breast feeding women;
- Mental or cognitive disorders;
Key Trial Info
Start Date :
October 1 2016
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 30 2019
Estimated Enrollment :
354 Patients enrolled
Trial Details
Trial ID
NCT03372694
Start Date
October 1 2016
End Date
December 30 2019
Last Update
June 12 2019
Active Locations (1)
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1
YueYang Hosptial of Intergrated Traditional Chinese and Western Medicine,Shanghai University of Traditional Chinese Medicine
Shanghai, Shanghai Municipality, China, 200437