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Shenqi Fuzheng Injection for the Treatment of Cancer-related Fatigue in Patients(BCS) With Digestive Tract .

Primary Purpose

Carcinogenic Fatigue

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
shenqifuzheng injection
Sodium Chloride Injection 0.9%
Sponsored by
Livzon Pharmaceutical Group Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Carcinogenic Fatigue

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 1. Patients with gastric cancer, esophageal cancer or colorectal cancer diagnosed by pathology or cytology;
  • 2. Diagnostic criteria for cancer-related fatigue;
  • 3. Syndrome differentiation of Chinese medicine is a syndrome of lung temper;
  • 4. Estimated survival over 3 months;
  • 5. ECOG score is less than or equal to 3
  • 6. Age 18 ~ 80 years old;
  • 7. Non-surgical indications or reluctance to operate the surgical treatment;
  • 8. 70 g/L or higher HGB;
  • 9. Stop and chemotherapy for more than 1 month;
  • 10. The patient is willing to accept the treatment of the programme, and can follow the doctor's advice to take the medicine and comply with the patient.

Exclusion Criteria:

  • 1. Any situation that may hinder the subject from completing the clinical trial, including but not limited to serious, uncontrollable organic disease or infection:

    1. clinically significant cardiovascular diseases, such as heart failure (NYHA III-IV), uncontrolled coronary heart disease, cardiomyopathy, arrhythmia, etc.
    2. serious clinical infection of activity (greater than 3 degrees nci-ctcae 4.03)
    3. uncontrolled hypertension (systolic pressure is greater than 160 mmHg or diastolic pressure is greater than 100 mmHg, despite the best drug treatment);
    4. severe liver and kidney function abnormality (blood creatinine is greater than 1.5 times ULN; ALT or AST is greater than 5 times ULN; Bilirubin is greater than 1.5 times ULN.
    5. other diseases that need to be controlled: pulmonary congestion, etc.
  • 2. Patients with symptoms, uncontrollable nerves, mental illness or mental disorders;
  • 3. Compliance.

Sites / Locations

  • First affiliated hospital of guangzhou university of traditional Chinese medicineRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

shenqifuzheng

0.9%sodium chloride

Arm Description

Outcomes

Primary Outcome Measures

Piper Fatigue Scale(PFS)
Change From Baseline in Piper Fatigue Scores at 42 days

Secondary Outcome Measures

Full Information

First Posted
December 26, 2017
Last Updated
March 5, 2018
Sponsor
Livzon Pharmaceutical Group Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT03456609
Brief Title
Shenqi Fuzheng Injection for the Treatment of Cancer-related Fatigue in Patients(BCS) With Digestive Tract .
Official Title
The Efficacy and Safety of Shenqi Fuzheng Injection for the Treatment of Cancer-related Fatigue in Patients(Palliative Care) With Digestive Tract Were Prospectively, Randomized Blind, Multicenter Clinical Trials
Study Type
Interventional

2. Study Status

Record Verification Date
December 2017
Overall Recruitment Status
Unknown status
Study Start Date
January 18, 2018 (Actual)
Primary Completion Date
December 30, 2019 (Anticipated)
Study Completion Date
December 30, 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Livzon Pharmaceutical Group Inc.

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
The efficacy and safety of cancer patients in patients with gastrointestinal cancer (Palliative care) in patients with gastrointestinal tumor (chemotherapy) were prospectively, randomized blind, multicenter clinical trials. They were randomly divided into 2 groups, test group Shenqifuzheng injection of 500 ml, the control group 0.9% sodium chloride injection, 500 ml, intravenous drip, 1 times a day, 14 days post, rest is 7 days, 21 days each for a period of treatment, observation of two procedures. At the same time, according to the NCCN guide and the health ministry issued the diagnosis and treatment guidelines for cancer treatment. The main curative effect of the clinic was to evaluate the pretreatment of cancer due to the fatigue score of the patients before and after treatment -- the Piper fatigue revision scale was used to evaluate the Chinese version. Assess effectiveness and safety based on clinical assessment
Detailed Description
Factors for the purpose of this study by observing theShenqifuzheng injection before and after treatment in patients with carcinoma due to fatigue scale scores, the classification of syndromes, the quality of life score changes and related laboratory index, evaluation factors ginseng and astragalus injection on the digestive tract tumor (chemotherapy) in patients with cancer-related fatigue and quality of life improved efficacy and safety. The experimental group was randomly divided into 2 groups, experimental group Shenqifuzheng injection of 500 ml. The control group was 0.9% sodium chloride injection, 500ml, intravenous drip, 1 time daily, 14 days for continuous use, 7 days of rest, and 1 treatment for each 21 days, and 2 courses were observed. At the same time, according to the NCCN guide and the health ministry issued the diagnosis and treatment guidelines for cancer treatment. Main efficacy evaluation indexes before and after treatment for cancer-related fatigue rating - adopting the Piper fatigue scale revised Chinese version, compare the experimental group and the control group before and after treatment cancer-related fatigue rating difference have differences. Secondary efficacy evaluation index to compare the ECOG score difference before and after the treatment, the quality of life score difference before and after the treatment, TCM syndrome curative effect, single symptom curative effect of immune function, tumors had curative effect (if any) and chemotherapy completion. Safety assessment includes the observation of vital signs, blood routine, urinary routine, routine stool, liver function, renal function, electrocardiogram examination, and adverse reactions during the treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Carcinogenic Fatigue

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
shenqifuzheng
Arm Type
Experimental
Arm Title
0.9%sodium chloride
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
shenqifuzheng injection
Intervention Description
500ml shenqifuzheng daily(at day 1-14 and day22-36)through intravenous infusion.
Intervention Type
Drug
Intervention Name(s)
Sodium Chloride Injection 0.9%
Intervention Description
500ml sodium chloride(0.9%)daily(at day 1-14 and day22-36)through intravenous infusion.
Primary Outcome Measure Information:
Title
Piper Fatigue Scale(PFS)
Description
Change From Baseline in Piper Fatigue Scores at 42 days
Time Frame
42 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 1. Patients with gastric cancer, esophageal cancer or colorectal cancer diagnosed by pathology or cytology; 2. Diagnostic criteria for cancer-related fatigue; 3. Syndrome differentiation of Chinese medicine is a syndrome of lung temper; 4. Estimated survival over 3 months; 5. ECOG score is less than or equal to 3 6. Age 18 ~ 80 years old; 7. Non-surgical indications or reluctance to operate the surgical treatment; 8. 70 g/L or higher HGB; 9. Stop and chemotherapy for more than 1 month; 10. The patient is willing to accept the treatment of the programme, and can follow the doctor's advice to take the medicine and comply with the patient. Exclusion Criteria: 1. Any situation that may hinder the subject from completing the clinical trial, including but not limited to serious, uncontrollable organic disease or infection: clinically significant cardiovascular diseases, such as heart failure (NYHA III-IV), uncontrolled coronary heart disease, cardiomyopathy, arrhythmia, etc. serious clinical infection of activity (greater than 3 degrees nci-ctcae 4.03) uncontrolled hypertension (systolic pressure is greater than 160 mmHg or diastolic pressure is greater than 100 mmHg, despite the best drug treatment); severe liver and kidney function abnormality (blood creatinine is greater than 1.5 times ULN; ALT or AST is greater than 5 times ULN; Bilirubin is greater than 1.5 times ULN. other diseases that need to be controlled: pulmonary congestion, etc. 2. Patients with symptoms, uncontrollable nerves, mental illness or mental disorders; 3. Compliance.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
lin lizhu, Dr.
Phone
13501505588
Email
13501505588@139.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
lin lizhu, Dr.
Organizational Affiliation
First affiliated hospital of guangzhou university of traditional Chinese medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
First affiliated hospital of guangzhou university of traditional Chinese medicine
City
Guangzhou
State/Province
Guangdong
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
lin lizhu, Dr.
Phone
13501505588
Email
13501505588@163.com

12. IPD Sharing Statement

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Shenqi Fuzheng Injection for the Treatment of Cancer-related Fatigue in Patients(BCS) With Digestive Tract .

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