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Herbal Treatment to Improve Chemotherapy Delivery (HATCHED)

Primary Purpose

Colon Cancer

Status
Unknown status
Phase
Phase 3
Locations
China
Study Type
Interventional
Intervention
Tonifying Spleen and Kidney Sequential Regimen
Placebo of 'Tonifying Spleen and Kidney Sequential Regimen
Sponsored by
Xiyuan Hospital of China Academy of Chinese Medical Sciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Colon Cancer focused on measuring Colon Cancer, Traditional Chinese Medicine, Adverse Effect of Chemotherapy, Chemotherapy

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patient with pathological diagnosis of colon cancer; no residual tumor at the resection margin.
  • tumor-node-metastasis(TNM)Stage II (high-risk)or III colon cancer according to 8th edition of American Joint Committee on Cancer(AJCC)Staging Manual. High-risk stage II disease is characterized by at least one of the following:

    1. T4 tumor,
    2. inadequately sampled nodes (<12 lymph nodes),
    3. clinical presentation with bowel obstruction or perforation,
    4. poorly differentiated histology ,exclusive of those cancers that are High degree of microsatellite instability(MSI-H),
    5. lymphovascular invasion,perineural invasion(PNI).
  • Underwent radical surgery no more than six weeks ago and plan to start chemotherapy.
  • Have not been enrolled in other therapeutic clinical trials within the near 30 days.
  • Age between 18 to 75 years; All genders; Eastern Cooperative Oncology Group - performance status(ECOG-PS)from 0 to 2; Women who are pregnant, lactating or of reproductive age are not eligible, while those of reproductive age using secure contraceptives are eligible.
  • No history of previous malignancy other than adequately treated in situ carcinoma of the uterine cervix or basal or squamous cell carcinoma of the skin, unless there has been a disease-free interval of at least 5 years.
  • Laboratory testing: blood routine examination: WBC≥3.5×109/L,NEUT≥1.5×109/L,PLT≥100×109/L,HGB≥90g/L;biochemical tests:TBIL≤1.5×ULN,AST(SGOT),ALT(SGPT)≤2.5×ULN,Scr≤1.5×ULN;CEA after surgery was normal.
  • Consented.
  • Agree not to be enrolled in other interventional studies during the research.

Exclusion Criteria:

  • Patients not suitable for chemotherapy of CapeOX ,which will be determined by the investigator or the attending physician.
  • Clinically relevant cardiovascular and/or cerebrovascular disease,active hepatitis,severe abnormalities in liver/ renal function tests.
  • Known allergy to any of the components of study drug.
  • Those who cannot take the study drug orally because of bowel obstruction and/or require for peripheral vein nutrition.
  • Malabsorption or diseases that affect the absorption.
  • Unstable situations or situations that may endanger the safety of patients and their compliance, such as severe mental illness,schizophrenia.
  • Colostomy

Sites / Locations

  • Beijing Chao Yang HospitalRecruiting
  • Civil Aviation General HospitalRecruiting
  • Oncology Department of Xiyuan Hospital of China Academy of Chinese Medical SciencesRecruiting
  • Beijing Cancer HospitalRecruiting
  • Chongqing University Cancer HospitalRecruiting
  • Guangdong Provincial Hospital of Traditional Chinese MedicineRecruiting
  • The Third People's Hospital of ZhengzhouRecruiting
  • Henan Provincial People's HospitalRecruiting
  • Zhengzhou Hospital of Traditional Chinese MedicineRecruiting
  • Jiangsu Province Hospital of Traditional Chinese MedicineRecruiting
  • Shanghai Zhongshan HospitalRecruiting
  • Tianjin Union Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

TCM group

Placebo group

Arm Description

Tonifying Spleen and Kidney Sequential Regimen(TSKSR) will be prescribed to the participants in each course of chemotherapy.

Placebo of Tonifying Spleen and Kidney Sequential Regimen(TSKSR)similar in color,smell and texture with TSKSR will be prescribed to participants in each course of chemotherapy.

Outcomes

Primary Outcome Measures

Completion Rate of 8-cycle Adjuvant Chemotherapy
Completion Rate of 8-cycle Adjuvant Chemotherapy=number of participants completing 8-cycle adjuvant chemotherapy/number of participants randomized to each group*100%

Secondary Outcome Measures

Completion Rate of Adjuvant Chemotherapy of Each Participant
Completion Rate of Adjuvant Chemotherapy of Each Participant=number of the last courses of chemotherapy/8*100%
Completion Rate of 4-cycle Adjuvant Chemotherapy
Completion Rate of 4-cycle Adjuvant Chemotherapy=number of participants completing 4-cycle adjuvant chemotherapy/number of participants randomized to each group*100%
Time to Treatment Failure,TTF
TTF is the period from randomization to the earliest day of an event such as withdrawal from protocol treatment for any reasons, patients refusal and loss to follow-up.
Relative Dose Intensity (RDI) of Adjuvant Chemotherapy
Relative dose intensity (RDI) (%) = (actual dose/ initial dose of adjuvant chemotherapy) × 100%
Proportion of Modifications of Time
Proportion of Modifications of Time=number of participants delaying chemotherapy /number of participants randomized to each group*100%.Delay is defined as ≥7days because of adverse event,such as weakness, myelosuppression, gastrointestinal reactions and other toxicity,except for administrative issues related to hospitalization.
Time of Dose Reductions of Adjuvant Chemotherapy for the First Time
It is the period from randomization to when a chemo-induced grade 3-4 granulocytopenia and/or a chemo-induced grade 2 thrombocytopenia is observed in participants for the first time,in which case,the dose of both Oxaliplatin and Capecitabine will be reduced by 25% of planned dosage.
Time of Dose Reductions of Adjuvant Chemotherapy for the Second Time
It is the period from randomization to when a chemo-induced grade 3-4 granulocytopenia and/or a chemo-induced grade 2 thrombocytopenia is observed in participants for the second time,in which case,the dose of both Oxaliplatin and Capecitabine will be reduced by 50% of planned dosage.
Proportion of Salvage Treatment
Proportion of Salvage Treatment=Number of participants receiving salvage treatment/Number of participants randomized to each group*100%.
Incidence of a Chemo-induced Grade 3-4 Nausea/Vomiting
Incidence of a Chemo-induced Grade 2 Diarrhea
Changes of Participants' ESAS Score
Edmonton Symptom Assessment Scale(ESAS) score will be used to evaluate the change of participants' QoL during adjuvant chemotherapy.ESAS has 9 items designed to assess the severity of commonly reported symptoms experienced by cancer patients,including pain, fatigue, drowsiness, nausea, dyspnea, depression, anxiety, well-being, and loss of appetite.Each items ranges from 0 to 10.
Changes of Participants' FACT-C Score
Functional Assessment of Cancer Therapy-Colorectal (FACT-C) score will be used to evaluate the change of participants' QoL during adjuvant chemotherapy.The FACT-C consists of 36 items,in four domains of well-being (physical,emotional,social,and functional),on a scale of 0 to 4.
Changes of TCM Symptoms Score
Based on a prior expert consensus,11 TCM symptoms were considered to be the most common symptoms during CapeOX chemotherapy,including vomiting, numbness, diarrhea, constipation, sensation of chill, nocturia, forgetfulness, spontaneous sweating, night sweats, dry mouth and canker sores, each of which ranges from 0 to 10.
Changes of Spleen Deficiency Scale Score
Based on prior researches,the investigator designed Spleen Deficiency Scale,which includes 8 items involving appetite,abdominal distension and so on.Each question ranges from 1 to 5.
Changes of Kidney Deficiency Scale Score
Based on prior researches,the investigator designed Kidney Deficiency Scale, which includes 8 items involving soreness of waist, tinnitus, and so on. Each question ranged from 1 to 5.
Incidence of AEs
Adverse effects(AEs) includes abnormal results of blood/urine/stool routine examination, liver/renal function test and electrocardiograms.
Incidence of SAEs
Serious Adverse effects(SAEs) includes abnormal results of blood/urine/stool routine examination, liver/renal function test and electrocardiograms.

Full Information

First Posted
October 14, 2018
Last Updated
January 9, 2021
Sponsor
Xiyuan Hospital of China Academy of Chinese Medical Sciences
Collaborators
Beijing University of Chinese Medicine, Peking University Third Hospital, Beijing Chao Yang Hospital, Jiangsu Province Hospital of Traditional Chinese Medicine, Shanghai Zhongshan Hospital, Guangdong Provincial Hospital of Traditional Chinese Medicine, Tianjin Union Medical Center, Henan Provincial People's Hospital, Zhengzhou Hospital of Traditional Chinese Medicine, Peking University Cancer Hospital & Institute, Chongqing University Cancer Hospital, Civil Aviation General Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03716518
Brief Title
Herbal Treatment to Improve Chemotherapy Delivery
Acronym
HATCHED
Official Title
Effect of TCM-TSKSR on Completion Rates of Chemotherapy in Patients With Stage II & III Colon Cancer: A Randomized Placebo-Controlled Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
November 2020
Overall Recruitment Status
Unknown status
Study Start Date
December 12, 2018 (Actual)
Primary Completion Date
May 31, 2021 (Anticipated)
Study Completion Date
May 31, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Xiyuan Hospital of China Academy of Chinese Medical Sciences
Collaborators
Beijing University of Chinese Medicine, Peking University Third Hospital, Beijing Chao Yang Hospital, Jiangsu Province Hospital of Traditional Chinese Medicine, Shanghai Zhongshan Hospital, Guangdong Provincial Hospital of Traditional Chinese Medicine, Tianjin Union Medical Center, Henan Provincial People's Hospital, Zhengzhou Hospital of Traditional Chinese Medicine, Peking University Cancer Hospital & Institute, Chongqing University Cancer Hospital, Civil Aviation General Hospital

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 designed to:(1) determine the efficacy of Traditional Chinese Medicine (TCM) 'Tonifying Spleen and Kidney Sequential Regimen' (TSKSR) in improving the completion rate of 8-cycle CapeOX chemotherapy in patients with stage II (high-risk)& III colon cancer;(2) evaluate the efficacy of the TCM-TSKSR on adverse events of CapeOX chemotherapy and it's impact on patients' quality of life (QoL).A randomized,double-blinded,placebo-controlled clinical trial including seven centers will be conducted in Mainland China.The study will enroll patients with stage II (high-risk)& III colon cancer who have completed radical surgery and are going to receive CapeOX chemotherapy.All participants will receive chemotherapy as prescribed by their treating physicians and be randomly assigned to either concurrent use of TCM-TSKSR or placebo.
Detailed Description
CapeOX chemotherapy is a combination therapy of Oxaliplatin 130mg/m^2 IV on 1st day and Capecitabine 1000mg/m^2 PO twice daily from 1th day to 14th day,21 days for each course of treatment.Adverse effects of chemotherapy,such as myelosuppression and gastrointestinal reactions,may lead to dose reductions,treatment delays or even discontinuation among cancer patients. According to IDEA study,the completion rate of 8-cycle CapeOX chemotherapy in colorectal cancer patients is 64%,which means that nearly 4 in 10 patients could not complete adjuvant chemotherapy as planned,which may negatively impact patients' survival outcomes.Some prior studies have shown that TCM can improve patients' symptom control and QoL during adjuvant chemotherapy,which may further improve the completion of adjuvant chemotherapy. However,there is a lack of definitive evidence to evaluate the effects of TCM in stage II(high-risk)& III colon cancer patients who receive adjuvant chemotherapy after radical surgery.The study will be conducted between 2018 and 2021.Four hundred participants will be enrolled and randomly assigned to either the experimental group or the control group.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colon Cancer
Keywords
Colon Cancer, Traditional Chinese Medicine, Adverse Effect of Chemotherapy, Chemotherapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
400 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
TCM group
Arm Type
Experimental
Arm Description
Tonifying Spleen and Kidney Sequential Regimen(TSKSR) will be prescribed to the participants in each course of chemotherapy.
Arm Title
Placebo group
Arm Type
Placebo Comparator
Arm Description
Placebo of Tonifying Spleen and Kidney Sequential Regimen(TSKSR)similar in color,smell and texture with TSKSR will be prescribed to participants in each course of chemotherapy.
Intervention Type
Drug
Intervention Name(s)
Tonifying Spleen and Kidney Sequential Regimen
Other Intervention Name(s)
TSKSR
Intervention Description
TSKSR will be given to the participants as follows:Liu-jun-an-wei Granule,1 pack each time,twice a day,PO,from 0 to 6th day of chemotherapy and Qi-tu-er-zhi Granule,1 pack each time,twice a day,PO,from 7th to 20th day of chemotherapy.
Intervention Type
Drug
Intervention Name(s)
Placebo of 'Tonifying Spleen and Kidney Sequential Regimen
Other Intervention Name(s)
Placebo of TSKSR
Intervention Description
Placebo of TCM-TSKSR will be given to the participants as follows:placebo of Liu-jun-an-wei Granule,1 pack each time,twice a day,PO,from 0 to 6th day of chemotherapy and placebo of Qi-tu-er-zhi Granule,1 pack each time,twice a day,from 7th to 20th day of chemotherapy.
Primary Outcome Measure Information:
Title
Completion Rate of 8-cycle Adjuvant Chemotherapy
Description
Completion Rate of 8-cycle Adjuvant Chemotherapy=number of participants completing 8-cycle adjuvant chemotherapy/number of participants randomized to each group*100%
Time Frame
6months
Secondary Outcome Measure Information:
Title
Completion Rate of Adjuvant Chemotherapy of Each Participant
Description
Completion Rate of Adjuvant Chemotherapy of Each Participant=number of the last courses of chemotherapy/8*100%
Time Frame
6months
Title
Completion Rate of 4-cycle Adjuvant Chemotherapy
Description
Completion Rate of 4-cycle Adjuvant Chemotherapy=number of participants completing 4-cycle adjuvant chemotherapy/number of participants randomized to each group*100%
Time Frame
3months
Title
Time to Treatment Failure,TTF
Description
TTF is the period from randomization to the earliest day of an event such as withdrawal from protocol treatment for any reasons, patients refusal and loss to follow-up.
Time Frame
6months
Title
Relative Dose Intensity (RDI) of Adjuvant Chemotherapy
Description
Relative dose intensity (RDI) (%) = (actual dose/ initial dose of adjuvant chemotherapy) × 100%
Time Frame
6months
Title
Proportion of Modifications of Time
Description
Proportion of Modifications of Time=number of participants delaying chemotherapy /number of participants randomized to each group*100%.Delay is defined as ≥7days because of adverse event,such as weakness, myelosuppression, gastrointestinal reactions and other toxicity,except for administrative issues related to hospitalization.
Time Frame
6months
Title
Time of Dose Reductions of Adjuvant Chemotherapy for the First Time
Description
It is the period from randomization to when a chemo-induced grade 3-4 granulocytopenia and/or a chemo-induced grade 2 thrombocytopenia is observed in participants for the first time,in which case,the dose of both Oxaliplatin and Capecitabine will be reduced by 25% of planned dosage.
Time Frame
6months
Title
Time of Dose Reductions of Adjuvant Chemotherapy for the Second Time
Description
It is the period from randomization to when a chemo-induced grade 3-4 granulocytopenia and/or a chemo-induced grade 2 thrombocytopenia is observed in participants for the second time,in which case,the dose of both Oxaliplatin and Capecitabine will be reduced by 50% of planned dosage.
Time Frame
6months
Title
Proportion of Salvage Treatment
Description
Proportion of Salvage Treatment=Number of participants receiving salvage treatment/Number of participants randomized to each group*100%.
Time Frame
6months
Title
Incidence of a Chemo-induced Grade 3-4 Nausea/Vomiting
Time Frame
6 months
Title
Incidence of a Chemo-induced Grade 2 Diarrhea
Time Frame
6 months
Title
Changes of Participants' ESAS Score
Description
Edmonton Symptom Assessment Scale(ESAS) score will be used to evaluate the change of participants' QoL during adjuvant chemotherapy.ESAS has 9 items designed to assess the severity of commonly reported symptoms experienced by cancer patients,including pain, fatigue, drowsiness, nausea, dyspnea, depression, anxiety, well-being, and loss of appetite.Each items ranges from 0 to 10.
Time Frame
6 months
Title
Changes of Participants' FACT-C Score
Description
Functional Assessment of Cancer Therapy-Colorectal (FACT-C) score will be used to evaluate the change of participants' QoL during adjuvant chemotherapy.The FACT-C consists of 36 items,in four domains of well-being (physical,emotional,social,and functional),on a scale of 0 to 4.
Time Frame
6months
Title
Changes of TCM Symptoms Score
Description
Based on a prior expert consensus,11 TCM symptoms were considered to be the most common symptoms during CapeOX chemotherapy,including vomiting, numbness, diarrhea, constipation, sensation of chill, nocturia, forgetfulness, spontaneous sweating, night sweats, dry mouth and canker sores, each of which ranges from 0 to 10.
Time Frame
6months
Title
Changes of Spleen Deficiency Scale Score
Description
Based on prior researches,the investigator designed Spleen Deficiency Scale,which includes 8 items involving appetite,abdominal distension and so on.Each question ranges from 1 to 5.
Time Frame
6months
Title
Changes of Kidney Deficiency Scale Score
Description
Based on prior researches,the investigator designed Kidney Deficiency Scale, which includes 8 items involving soreness of waist, tinnitus, and so on. Each question ranged from 1 to 5.
Time Frame
6months
Title
Incidence of AEs
Description
Adverse effects(AEs) includes abnormal results of blood/urine/stool routine examination, liver/renal function test and electrocardiograms.
Time Frame
6months
Title
Incidence of SAEs
Description
Serious Adverse effects(SAEs) includes abnormal results of blood/urine/stool routine examination, liver/renal function test and electrocardiograms.
Time Frame
6months

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: Patient with pathological diagnosis of colon cancer; no residual tumor at the resection margin. tumor-node-metastasis(TNM)Stage II (high-risk)or III colon cancer according to 8th edition of American Joint Committee on Cancer(AJCC)Staging Manual. High-risk stage II disease is characterized by at least one of the following: T4 tumor, inadequately sampled nodes (<12 lymph nodes), clinical presentation with bowel obstruction or perforation, poorly differentiated histology ,exclusive of those cancers that are High degree of microsatellite instability(MSI-H), lymphovascular invasion,perineural invasion(PNI). Underwent radical surgery no more than six weeks ago and plan to start chemotherapy. Have not been enrolled in other therapeutic clinical trials within the near 30 days. Age between 18 to 75 years; All genders; Eastern Cooperative Oncology Group - performance status(ECOG-PS)from 0 to 2; Women who are pregnant, lactating or of reproductive age are not eligible, while those of reproductive age using secure contraceptives are eligible. No history of previous malignancy other than adequately treated in situ carcinoma of the uterine cervix or basal or squamous cell carcinoma of the skin, unless there has been a disease-free interval of at least 5 years. Laboratory testing: blood routine examination: WBC≥3.5×109/L,NEUT≥1.5×109/L,PLT≥100×109/L,HGB≥90g/L;biochemical tests:TBIL≤1.5×ULN,AST(SGOT),ALT(SGPT)≤2.5×ULN,Scr≤1.5×ULN;CEA after surgery was normal. Consented. Agree not to be enrolled in other interventional studies during the research. Exclusion Criteria: Patients not suitable for chemotherapy of CapeOX ,which will be determined by the investigator or the attending physician. Clinically relevant cardiovascular and/or cerebrovascular disease,active hepatitis,severe abnormalities in liver/ renal function tests. Known allergy to any of the components of study drug. Those who cannot take the study drug orally because of bowel obstruction and/or require for peripheral vein nutrition. Malabsorption or diseases that affect the absorption. Unstable situations or situations that may endanger the safety of patients and their compliance, such as severe mental illness,schizophrenia. Colostomy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yufei Yang, M.D.
Phone
8613701366913
Email
yyfwdbwyy@126.com
First Name & Middle Initial & Last Name or Official Title & Degree
Yun Xu, M.D.
Phone
8615210775378
Email
xyxiao78@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yufei Yang, M.D.
Organizational Affiliation
Xi-Yuan Hospital, China Academy of Chinese Medical Sciences
Official's Role
Principal Investigator
Facility Information:
Facility Name
Beijing Chao Yang Hospital
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100020
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Minzhe Li, M.D.
Facility Name
Civil Aviation General Hospital
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100025
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jianping Cheng
Facility Name
Oncology Department of Xiyuan Hospital of China Academy of Chinese Medical Sciences
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100091
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yun Xu, M.D.
Phone
86 10 62835355
Email
xyxiao78@163.com
First Name & Middle Initial & Last Name & Degree
Yufei Yang, M.D.
Phone
86 10 62835355
Email
yyfwdbwyy@126.com
Facility Name
Beijing Cancer Hospital
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100142
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Aiwen Wu, M.D.
Phone
13911577190
Facility Name
Chongqing University Cancer Hospital
City
Chongqing
State/Province
Chongqing
ZIP/Postal Code
400030
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Wei Wang
Facility Name
Guangdong Provincial Hospital of Traditional Chinese Medicine
City
Guangdong
State/Province
Guangzhou
ZIP/Postal Code
510120
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jin Wan, M.D.
Facility Name
The Third People's Hospital of Zhengzhou
City
Zhengzhou
State/Province
Henan
ZIP/Postal Code
450000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yang Cao
Facility Name
Henan Provincial People's Hospital
City
Zhengzhou
State/Province
Henan
ZIP/Postal Code
450003
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Shundong Cang, M.D.
Phone
13592675836
Facility Name
Zhengzhou Hospital of Traditional Chinese Medicine
City
Zhengzhou
State/Province
Henan
ZIP/Postal Code
450007
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Baozhu Zeng
Phone
13838520891
Facility Name
Jiangsu Province Hospital of Traditional Chinese Medicine
City
Nanjing
State/Province
Jiangsu
ZIP/Postal Code
210029
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Peng Shu, M.D.
Facility Name
Shanghai Zhongshan Hospital
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200032
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Tianshu Liu, M.D.
Facility Name
Tianjin Union Medical Center
City
Tianjin
State/Province
Tianjin
ZIP/Postal Code
300121
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Huaqing Wang, M.D.

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34432206
Citation
Zhang T, Fei YT, Xu Y, Sun LY, He B, Yan SH, Tang M, Yan YZ, Mao J, Yang YF. Effect of Jianpi Bushen Sequential Formula on Adjuvant Chemotherapy of Colon Cancer: Study Protocol for a Randomized Controlled Trial. Chin J Integr Med. 2021 Dec;27(12):891-895. doi: 10.1007/s11655-021-3448-9. Epub 2021 Aug 25.
Results Reference
derived

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