Treatment of CRF With Syndrome Differentiation of TCM

Chronic Respiratory Failure Clinical Trial

Official title:

An Exploratory Clinical Study on Reducing AECOPD of Chronic Respiratory Failure With COPD by Syndrome Differentiation

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT04694755
• Other study ID #: Treatment of CRF with TCM
• Status: Not yet recruiting
• Phase: Early Phase 1
• Start date: January 2021
• Est. completion date: October 2022

Study information

• Verified date: August 2020
• Source: Henan University of Traditional Chinese Medicine
• Contact: Minghang Wang, doctor
• Phone: 18638392188
• Email: wmh107hn[@]163.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Taking the patients with chronic respiratory failure caused by COPD as the research object and the acute exacerbation of COPD as the main outcome index, the investigators hope to establish the syndrome differentiation and treatment scheme of COPD treated by traditional Chinese medicine, reduce the acute exacerbation of AECOPD, improve the clinical symptoms, improve the quality of life, reduce the mortality, preliminarily explore the mechanism of action, and lay the foundation for further research.

Description:

Chronic respiratory failure of chronic obstructive pulmonary disease belongs to the category of "lung distention", "asthma syndrome", "dyspnea" and "phlegm drink" in traditional Chinese medicine. According to traditional Chinese medicine, the pathology of this disease is mainly the dysfunction of lung ventilation. The basic pathogenesis is that the viscera are repeatedly affected by evil, the lung qi is damaged due to long-term disease, the lung function is damaged, the air mechanism is blocked, the application is publicized, the phlegm is turbid, the blood stasis is inevitable for a long time, and the lung qi is further damaged. The main clinical manifestations are shortness of breath, wheezing, shortness of breath, superficial shortness of breath and "drama of wheezing when moving", which may be accompanied by cough, expectoration, chest tightness, palpitation, lips, purple darkness, swelling of floating limbs, etc. The treatment of chronic respiratory failure patients with COPD can be significantly improved clinical symptoms such as shortness of breath and wheezing, reduce the number of acute exacerbations of patients, but there is still a lack of high-level evidence-based medicine research. Therefore, this project puts forward the hypothesis that "syndrome differentiation therapy can reduce AECOPD of COPD".It is proposed to adopt a multicenter, randomized, double-blind, placebo-controlled trial design, taking the patients with chronic respiratory failure caused by chronic obstructive pulmonary disease as the research object. The patients who meet the inclusion criteria, are divided into heart lung qi deficiency and lung kidney qi deficiency according to syndrome differentiation. The participants are randomly divided into the experimental group of 60 cases and the control group of 60 cases. The control group is given placebo treatment, and the experimental group is given Chinese medicine granules. The patients were followed up for 26 weeks. The main outcome indicators include the number of times of acute exacerbation of COPD, and the secondary outcome indicators include all-cause mortality, severity of acute exacerbation of COPD, clinical symptoms, CCQ score of COPD clinical questionnaire, quality of life score, dyspnea score, 6MWD, arterial blood gas analysis index, incidence and use time of mechanical ventilation, use time of oxygen therapy, serology index, health and economy Learning indicators, safety indicators, etc. To establish the TCM treatment scheme of chronic respiratory failure of COPD, reduce the acute aggravation of AECOPD, improve the clinical symptoms, improve the quality of life, reduce the mortality rate, preliminarily explore the mechanism of action, and lay the foundation for further research.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 120
• Est. completion date: October 2022
• Est. primary completion date: May 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 40 Years to 80 Years

Eligibility

Inclusion criteria

1. patients who meet the diagnostic criteria of COPD in stable stage;

2. patients whose blood gas analysis meets PaO2 < 60mmhg and / or PaCO2 > 50mmhg in calm breathing at sea level;

3. patients whose syndrome differentiation meets the syndrome of heart lung qi deficiency and lung kidney qi deficiency;

4. patients whose age is = 40 years and = 80 years;

5. patients who are willing to receive treatment and sign the informed consent.

exclusion criteria:

1. chronic respiratory failure caused by bronchial asthma, bronchiectasis, cystic pulmonary fibrosis, lung cancer and other respiratory diseases;

2. acute aggravation of the original chronic respiratory failure;

3. patients with tumor, serious cardiovascular and cerebrovascular diseases (acute myocardial infarction, cardiac function level 3 and above, stroke, cerebral hemorrhage, etc.) and serious liver and kidney diseases (serious liver disease refers to liver cirrhosis, portal hypertension and varicose bleeding, and serious kidney disease includes dialysis and kidney transplantation) and other people who cannot participate in clinical research;

4. pregnant and lactating women;

5. patients with mental diseases and mental disorders;

6. those who are participating in clinical trials of other drugs, known to be allergic to treatment drugs.

Related Conditions & MeSH terms

• Chronic Respiratory Failure
• Respiratory Insufficiency

Intervention

Drug:
• Placebo
On the basis of dextrin and bitter agent, 5% of the drug was used to prepare.Its appearance, weight, color and smell are basically the same as traditional Chinese medicine granule.Tianjiang brand formula granules, in line with GMP standards
• Traditional Chinese medicine prescription
Tianjiang brand formula granules, in line with GMP standards

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Henan University of Traditional Chinese Medicine

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Frequency of acute exacerbation	It will be assessed by frequencies of AECOPD-related hospitalizations.	Up to week 52.
Primary	Duration of acute exacerbation	Duration of acute exacerbation will be recorded.	Up to week 52.
Secondary	All-cause mortality	The all-cause mortality will be calculated in each group at the end of the trial.	up to 52 weeks.
Secondary	Dyspnea	Dyspnea will be assessed by modified Medical Research Council (mMRC) scores set up by American Thoracic Society. A score of 0-4 will be given according to the degree of immediate dyspnea. A higher score indicates a worse dyspnea.	Change from baseline mMRC scores at week 4, 13, 26, 39 and 52.
Secondary	COPD assessment test (CAT)	CAT will be used to evaluate quality of life. A total score of 0-40 will be given with a higher score indicating a worse condition.	Change from baseline CAT scores at week 4, 13, 26, 39 and 52.
Secondary	Clinical symptoms and Signs	Assessment will be performed by clinical symptom assessment questionnaire. The clinical symptoms to be evaluated in this study include cough, expectoration, chest tightness, shortness of breath, wheezing and cyanosis. A score of 0-3 will be given to every symptom or sign with a higher score indicating a worse conditoin.	Change from baseline clinical symptoms assessment questionnaire scores at week 4, 13, 26, 39 and 52.
Secondary	Six-minute walking distance(6MWD)	6MWD will be applied to evaluate the exercise capacity. The higher values indicate the better exercise capacity.	Change from baseline 6MWD at week 4, 13, 26, 39 and 52
Secondary	CCQ	Clinical symptom assessment questionnaire of COPD (CCQ) will be used to assess symptom. There are 10 items with a score of 0-6 for each item. A higher value will indicate a worse symptom.	Change from baseline clinical symptom assessment questionnaire scores at week 4, 13, 26, 39 and 52.
Secondary	FEV1	Forced expiratory volume in one second ( FEV1) will be applied to assess pulmonary function.	Change from baseline FEV1 at week 26 and 52.
Secondary	FVC	Forced vital capacity (FVC) will be applied to assess pulmonary function.	Change from baseline FVC at week 26 and 52.
Secondary	PaO2	Partial pressure of oxygen (PaO2) will be applied to assess artery blood gas. PaO2=60mmHg will indicatea the body is in a state of hypoxi.	Change from baseline ABG at week 13, 26, 39 and 52.
Secondary	PaCO2	Partial pressure of carbon dioxide (PaCO2) will be applied to assess artery blood gas. PaCO2=50mmHg will indicatea the body is in a state of carbon dioxide retention.	Change from baseline ABG at week 13, 26, 39 and 52.
Secondary	Duration of oxygen inhalation	Duration of oxygen inhalation will be used to evaluate quality of life. The longer the use, the worse the condition.	Change from baseline Duration of oxygen inhalation at week 4, 13, 26, 39 and 52.