TCM in the Treatment of Lung Adenocarcinoma
Primary Purpose
Lung Adenocarcinoma
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Jing-yan-kang Granule
PC chemotherapy and symptomatic treatment
Sponsored by
About this trial
This is an interventional treatment trial for Lung Adenocarcinoma
Eligibility Criteria
Inclusion Criteria:
- A confirmed diagnosis of LADC.
- Age ranges from17years to75years.
- A KPS score ≥40.
- Without radiotherapy, immunotherapy and targeted therapy.
- Without participanting in any other trial.
- With signed informed consent.
Exclusion Criteria:
- Pregnant, nursing or may become pregnant women.
- The patient has a history of allergy to any of the components of the intervention drug;
- Patients with severe liver and kidney dysfunction, cardiovascular and cerebrovascular diseases.
- Unconscious or unable to communicate normally.
- Patients with poor compliance.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Other
Arm Label
Experimental Group
Control Group
Arm Description
On the basis of PC chemotherapy and symptomatic treatment, the patients in the experimental group will receive jing-yuan-kang granule with one dose daily.
All the patients in control group will receive PC chemotherapy and symptomatic treatment without other treatment.
Outcomes
Primary Outcome Measures
The quality of life will be evaluated by The European Organization for Research and Treatment of Cancer Quality of life Questinnaire Core-30(EORTC QLQ-C30) scale
A score of 1-4 will be administrated for each item in EORTC QLQ-C30 . The higher scores will indicate the worse outcomes.
Quality of life will be evaluated by Quality of life Questinnaire Lung Cancer-13(QLQ-LC13)
A score of 1-4 will be administrated for each item in QLQ-LC13. The higher scores will indicate the worse outcomes.
Secondary Outcome Measures
Karnofsky(KPS) scores
Physical conditions will be evaluated by KPS scores with a score of 0-100. A higher score will indicate a better physical conditon.
TCM syndrome index
TCM symptom index will be recorded and calculated referring to the Guiding Principles of Clinical Research of New Chinese Medicine Treating Primary Bronchial Lung Cancer (2002 Edition) published by National Medical Products Administration of China. A total of scores of all the related symptoms will be calculated with a 0-4 for each symptom at baseline and after treatment. A higher value will indicate a worse symptom. The difference of TCM symptoms between baseline and posttreatment will be calculated first. Then, we will obtain the TCM syndrome index by the ratio between the above difference and the scores at baseline.
Change of tumor volume
Change of tumor volume will be assessed by the length of longest diameter. The longger diameter will indicate worse disease.
Adverse events will be evaluated and recorded at any time.
Safety
Full Information
NCT ID
NCT04482829
First Posted
July 3, 2020
Last Updated
July 18, 2020
Sponsor
Henan University of Traditional Chinese Medicine
1. Study Identification
Unique Protocol Identification Number
NCT04482829
Brief Title
TCM in the Treatment of Lung Adenocarcinoma
Official Title
Efficacy and Safety of Jing-yuan-kang Granule in the Treatment of Lung Adenocarcinoma
Study Type
Interventional
2. Study Status
Record Verification Date
July 2020
Overall Recruitment Status
Unknown status
Study Start Date
September 15, 2020 (Anticipated)
Primary Completion Date
December 30, 2020 (Anticipated)
Study Completion Date
June 30, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Henan University of Traditional Chinese Medicine
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study is to evaluate the efficacy and safety of Jin-yuan-kang granule in the treatment of lung adenocarcinoma (LUAD) preliminarily, and provide reference for further study.
Detailed Description
Lung adenocarcinoma (LUAD) is a type of non-small cell lung cancer (NSCLC) with a rapid disease progression and poor treatment effect. The LUAD patients have a short median survival time with 8-11 months. Up to now, chemotherapy is still the first-line treatment for LUAD. PC protocol (pemetrexed + cisplatin) is most commonly used, which is also recommended by NCCN guidelines. However, critical side effects have limited the application and efficacy. Patients will undergo poor quality of life, and the disease will progress rapidly. We still face the stern situation for the treatment of LUAD. It is urgent to develop new treatment and management strategies. Our previous study showed that jing-yuan-kang granule has certain curative effect on LUAD.
This is a multi-certers, randomized, controlled clinical trial to assess the efficacy and safety of Jing-yuan-kang granule in improving quality of life for LUAD patients. After a 2-week wash-out period, a total of 144 LUAD patients will be randomly assigned into experimental or control group with a ratio of 1:1. On the basis of that all the participants will receive PC chemotherapy and symptomatic treatment, the patients in the experimental group will receive jing-yuan-kang granule with no other treatments for control group. The primary outcome is quality of life. The secondary outcomes include Karnofsky (KPS) scores, clinical symptoms, and change of tumor volume. Safety and adverse events will also be assessed.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lung Adenocarcinoma
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
144 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Experimental Group
Arm Type
Experimental
Arm Description
On the basis of PC chemotherapy and symptomatic treatment, the patients in the experimental group will receive jing-yuan-kang granule with one dose daily.
Arm Title
Control Group
Arm Type
Other
Arm Description
All the patients in control group will receive PC chemotherapy and symptomatic treatment without other treatment.
Intervention Type
Drug
Intervention Name(s)
Jing-yan-kang Granule
Intervention Description
Jing-yuan-kang granule will be administered 6 days on and 1 days off for 12weeks.
Intervention Type
Drug
Intervention Name(s)
PC chemotherapy and symptomatic treatment
Intervention Description
Drugs used in PC chemotherapy includes Pemetrexed and Cisplatin. Pemetrexed disodium for injection 500 mg per square meter, intravenous drip on day 1 in each treatment cycle.
Cisplatin injection 75 mg per square meter, intravenous drip from day 1 to day 3 in each treatment cycle. One treatment cycle will be continued for 21 days and 4 cycles will be performed.
If necessary, symptomatic treatment will also be used.
Primary Outcome Measure Information:
Title
The quality of life will be evaluated by The European Organization for Research and Treatment of Cancer Quality of life Questinnaire Core-30(EORTC QLQ-C30) scale
Description
A score of 1-4 will be administrated for each item in EORTC QLQ-C30 . The higher scores will indicate the worse outcomes.
Time Frame
Change at 3 weeks, 6 weeks, 9 weeks, and 12 weeks after treatment compared to baseline.
Title
Quality of life will be evaluated by Quality of life Questinnaire Lung Cancer-13(QLQ-LC13)
Description
A score of 1-4 will be administrated for each item in QLQ-LC13. The higher scores will indicate the worse outcomes.
Time Frame
Change at 3 weeks, 6 weeks, 9 weeks, and 12 weeks after treatment compared to baseline.
Secondary Outcome Measure Information:
Title
Karnofsky(KPS) scores
Description
Physical conditions will be evaluated by KPS scores with a score of 0-100. A higher score will indicate a better physical conditon.
Time Frame
Change at 3 weeks, 6 weeks, 9 weeks, and 12 weeks after treatment compared to baseline.
Title
TCM syndrome index
Description
TCM symptom index will be recorded and calculated referring to the Guiding Principles of Clinical Research of New Chinese Medicine Treating Primary Bronchial Lung Cancer (2002 Edition) published by National Medical Products Administration of China. A total of scores of all the related symptoms will be calculated with a 0-4 for each symptom at baseline and after treatment. A higher value will indicate a worse symptom. The difference of TCM symptoms between baseline and posttreatment will be calculated first. Then, we will obtain the TCM syndrome index by the ratio between the above difference and the scores at baseline.
Time Frame
Change at 3 weeks, 6 weeks, 9 weeks, and 12 weeks after treatment compared to baseline.
Title
Change of tumor volume
Description
Change of tumor volume will be assessed by the length of longest diameter. The longger diameter will indicate worse disease.
Time Frame
Change at 12 weeks after treatment compared to baseline.
Title
Adverse events will be evaluated and recorded at any time.
Description
Safety
Time Frame
at baseline, up to 6 weeks and 12 weeks after treatment.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
A confirmed diagnosis of LADC.
Age ranges from17years to75years.
A KPS score ≥40.
Without radiotherapy, immunotherapy and targeted therapy.
Without participanting in any other trial.
With signed informed consent.
Exclusion Criteria:
Pregnant, nursing or may become pregnant women.
The patient has a history of allergy to any of the components of the intervention drug;
Patients with severe liver and kidney dysfunction, cardiovascular and cerebrovascular diseases.
Unconscious or unable to communicate normally.
Patients with poor compliance.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dan-dan Wei
Phone
+8613849186250
Email
1617924593@qq.com
First Name & Middle Initial & Last Name or Official Title & Degree
Shi-qing Jiang
Phone
+8613607640006
Email
jiangshiqing66@126.com
12. IPD Sharing Statement
Learn more about this trial
TCM in the Treatment of Lung Adenocarcinoma
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