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Impact of Chinese dialectical comprehensive program for changes in clinical symptoms of non-small cell lung cancer patients in Chemoradiation therapy mode: a prospective continuous tracking cohort study

Impact of Chinese dialectical comprehensive program for changes in clinical symptoms of non-small cell lung cancer patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OCH-13004245
Enrollment
Unknown
Registered
2013-12-04
Start date
2014-02-10
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

lung cancer

Interventions

control group:Routing chemo-radio therapy

Sponsors

Weifang Chinese Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: The patients signed informed consent, and have good compliance; (2)The patients who be considered as NSCLC due to clinical symptoms or CT, MRI and other non-invasive examination can be used as a pre-filter object; (3)Before pre-screening there is not any surgery, radiotherapy, chemotherapy, immunotherapy, and traditional Chinese medicine as an antitumor therap; (4) before the pre-screening, according to the RECIST criteria (Evaluation Criteria in Solid tumors) definition, there must be measurable disease; (5) after the pre-screening,stage I, II, III, IV non-small cell lung cancer patients who confirmed histologically or cytologically; (6) aged 18-75 years old;

Exclusion criteria

Exclusion criteria: (1) can not use language to express their demands or independent communicators; (2) women during pregnancy or breast-feeding, psychiatric patients, criminals, soldiers and other vulnerable groups; (3) According to the investigator's judgment, there is serious harm to patient safety, or concomitant diseases which affected patients to complete the study and may cause bias of the findings, such as combining interstitial lung disease, tuberculosis, blood diseases, heart disease, diabetes, hypertension and other chronic diseases or other malignancies; (4) treatment program will include surgery removal, biological immune therapy and EGFR inhibitors (EGFR TKI) persons; (5) researchers participating in other clinical.

Design outcomes

Secondary

MeasureTime frame
Measurable disease according to Response Evaluation;The quality of life according to FACT-L table;Toxic effects according to the RTOG radiation reaction;Pregression Free Survival time;Overall Survival;Median Survival Time;

Countries

China

Contacts

Public ContactChanggang Sun

Weifang Chinese Medicine Hospital

zhongliuyike@163.com+86 13583696099

Outcome results

None listed

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