Effect of Traditional Chinese Medicine on Outcomes in Patients With Severe Pneumonia

Phase 3

• Conditions: Community-Acquired Infections
• Interventions: Drug: TCM plus conventional drug; Drug: TCM placebo plus conventional drug

• Registration Number: NCT03185923
• Lead Sponsor: Henan University of Traditional Chinese Medicine

Brief Summary

This study evaluates the integrated traditional Chinese and Western medicine in the treatment of severe community acquired pneumonia in adults. Half of participants will receive traditional Chinese and Western medicine in combination, while the other half will receive a placebo traditional Chinese and Western medicine.

Detailed Description

Improving the care of patients with community-acquired pneumonia (CAP) has been the focus of many different organizations. Such efforts at improvement in care are warranted, because CAP, especially severe CAP remains the leading cause of death in the world. Despite advances in antimicrobial therapy, rates of mortality due to severe CAP have not decreased significantly since penicillin became routinely available.

traditional Chinese Medicine, has been used for thousands of years in treating pneumonia. To date, it has become popular and widely practiced in many countries around the world. In the past decades, Evidences from both clinicians and patients suggest that there is some beneficial effect of TCM on severe CAP.

At present, there are many therapies available for patients with severe CAP, it is difficult for us to identify the most suitable therapy. Thus, this study aims to compare the efficacy of combination conventional drug and TCM to the conventional drug and placebo, and then determine which one is the better therapy, providing a scientific basis for clinical decision.

This is a multi-center, randomized, controlled trial to compare the efficacy of two therapies for patients with severe CAP. 198 subjects will be randomly assigned to one therapies (conventional drug, and the combination of conventional drug and TCM) for 28 days treatment. After the treatment period, subjects in two arms will be followed up for 12 weeks. The primary outcomes will include treatment failure, and secondary outcomes Time to clinical stability, length hospital stays, in-hospital mortality, SOFA questionnaire, quality of life (CAP-PRO ) and health economics.

Study Timeline

• Status Verified: 2017-06
• Study First Submitted: 2017-06-04
• Study First Submitted QC: 2017-06-11
• Last Update Submitted: 2017-06-11
• Study First Posted: 2017-06-14
• Last Update Posted: 2017-06-14
• Study Start: 2017-06-20
• Primary Completion: 2019-12-31
• Study Completion: 2020-12-31

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 198

Inclusion Criteria

• were aged 18 years to 80 years.
• met severe community-acquired pneumonia criteria (defined by modified American Thoracic Society criteria).
• Syndrome differentiation meets criteria of phlegm-heat obstructing in the lung syndrome, pulmonary stagnation of phlegm syndrome, Pathogenic heat trapping the pericardium syndrome, or Pathogenic depression is taking off syndrome.

Exclusion Criteria

• Pregnant and lactating women.
• trauma, hematologic malignancies, various solid tumors, and obstetric complications.
• Aspiration pneumonia, fungal pneumonia, HIV related Pneumocystis carinii pneumonia, tuberculosis, Bronchiectasis with infection and pulmonary abscess;
• Dementia, mental disorders and reluctant partners.
• Be discharged from hospital within 2 days or require operation.
• reported severe immunosupression (human immunodeficiency virus infection, immunosuppressive conditions or medications).
• Neuromuscular disorders affecting respiratory motor function.
• Patients with severe cardiovascular，with severe liver and kidney disease.
• Patients who have participated in other clinical studies in the past 4 weeks.
• Patients unwilling to sign informed consent.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
TCM plus conventional drug	TCM plus conventional drug	The experimental group will receive three type of TCM inaddition conventional drug according to china CAP guidline 2016.
TCM placebo plus conventional drug	TCM placebo plus conventional drug	The control group will receive three type of placebo TCM inaddition conventional drug according to china CAP guidline 2016.

Primary Outcome Measures

Name	Time	Method
Treatment failure	up to 28 days.	The primary efficacy outcome was the rate of treatment failure, which includes treatment failure that occurred.

Secondary Outcome Measures

Name	Time	Method
time to clinical stability	up to 28 days.	Clinical stability
length hospital stays	up to 28 days.	length hospital stays will be recorded.
in-hospital mortality	up to 28 days.	in-hospital mortality will be recorded.
SOFA questionnaire	Change from baseline SOFA score at day 0、7、14、28 of the treatment phase.	Clinical symptom assessment questionnaire of severe CAP
CAP -CRO	Change from baseline CAP -CRO score at day 0、7、14、28 of the treatment phase.at week 4, week 8, week 12 of the follow-up phase.	CAP doctor reported outcome scale will be used to assess symptoms.
Health economics	up to 28 days.	Cost of the treatment phase will be recorded.

Trial Locations

Locations (1)

The First Affiliated Hospital of Henan University of Traditional Chinese Medicine; 🇨🇳 Zhengzhou, Henan, China