Effect of Jing Si Herbal Tea on Inflammation in Patients With Cardiovascular Disease

Sponsor
Buddhist Tzu Chi General Hospital (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05420987
Collaborator
(none)
100
2
30

Study Details

Study Description

Brief Summary

Jing Si herbal tea includes eight Chinese herbs: such as mugwort leaves, fish needle grass, Ophiopogon japonicus, platycodon, perilla leaves, chrysanthemum, and licorice. In vitro, these ingredients were found to be able to block the binding of SARS-CoV-2 and human ACE2 receptor, and further reduce the penetration ability of the virus. Now, Jing Si herbal tea liquid packets have obtained the special license for export from the Ministry of Health and Welfare in Taiwan.

The aim of the study is to investigate (1) the effect of Jing Si herbal tea liquid on blood pressure, blood sugar, and cholesterol in patients with cardiovascular diseases. (2)The human gut microbiota change which is associated with TMAO production (3) The proinflammatory and inflammatory biomarkers change.

We are going to recruit 100 participants from cardiovascular clinics, including patients with hypertension, hyperlipidemia, ischemic heart disease and diabetes, aged 20-75 years old. We exclude those who are cancer patients, have comorbidities with poor control, patients with eGFR< 40 ml/min/1.73m2, those who are pregnant, breastfeeding, and in their menstrual period when recruiting.

The study has two parts. The first part is a pilot study with 20 subjects all take active Jing Si herbal tea. The second part is a double-blind randomized controlled study with 40 subjects in each arm.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Jing Si herbal tea liquid packet
N/A

Detailed Description

Jing Si herbal tea includes eight Chinese herbs: such as mugwort leaves, fish needle grass, Ophiopogon japonicus, platycodon, perilla leaves, chrysanthemum, and licorice. In vitro, these ingredients were found to be able to block the binding of SARS-CoV-2 and human ACE2 receptor, and further reduce the penetration ability of the virus. Now, Jing Si herbal tea liquid packets have obtained the special license for export from the Ministry of Health and Welfare in Taiwan.

The aim of the study is to investigate (1) the effect of Jing Si herbal tea liquid on blood pressure, blood sugar, and cholesterol in patients with cardiovascular diseases. (2)The human gut microbiota change which is associated with TMAO production (3) The proinflammatory and inflammatory biomarkers change.

We are going to recruit 100 participants from cardiovascular clinics, including patients with hypertension, hyperlipidemia, ischemic heart disease and diabetes, aged 20-75 years old. We exclude those who are cancer patients, have comorbidities with poor control, patients with eGFR< 40 ml/min/1.73m2, those who are pregnant, breastfeeding, and in their menstrual period when recruiting.

The study has two parts. The first part is a pilot study with 20 subjects all take active Jing Si herbal tea. The second part is a double-blind randomized controlled study with 40 subjects in each arm.

All the patients' specimens and questionnaires are going to be collected on Day0, Day28, and Day84.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Supportive Care
Official Title:
The Effects of JING SI HERBAL TEA LIQ UID PACKETS on Inflammation in Patients With Cardiovascular Disease
Anticipated Study Start Date :
Jun 1, 2022
Anticipated Primary Completion Date :
Dec 1, 2024
Anticipated Study Completion Date :
Dec 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: active arm

Jing Si herbal tea liquid packet

Dietary Supplement: Jing Si herbal tea liquid packet
Jing Si herbal tea includes eight Taiwan native-grown herbs: such as mugwort leaves, fish needle grass, Ophiopogon japonicus, platycodon, perilla leaves, chrysanthemum, and licorice

Placebo Comparator: control arm

Jing Si herbal tea placebo

Dietary Supplement: Jing Si herbal tea liquid packet
Jing Si herbal tea includes eight Taiwan native-grown herbs: such as mugwort leaves, fish needle grass, Ophiopogon japonicus, platycodon, perilla leaves, chrysanthemum, and licorice

Outcome Measures

Primary Outcome Measures

  1. inflammatory biomarkers [3 months]

    IL-1b (pg/mL), IL-4(pg/mL), IL-6(pg/mL), IL-10(pg/mL), TNF-gamma(pg/mL),TNF-alpha (pg/mL)

  2. inflammatory biomarkers [3 months]

    GlycA (umol/L)

  3. lipid profile , Glu-AC, hs_CRP [3 months]

    Total cholesterol(mg/dL), TG(mg/dL), HDL-C(mg/dL), LDL-C(mg/dL), uric acid (mg/dL) and Glu-AC (mg/dL),hs_CRP(mg/dL)

  4. diabetes control index [3 months]

    HbA1c (%), insulin (mU/L), HOMA-IR, HOMA-beta

  5. biomarkers for congestive heart failure [3 months]

    Nt-proBNP (pg/ mL)

  6. heart function measurement for congestive heart failure [3 months]

    LVEF(%)

  7. kidney function 1 [3 months]

    BUN (mg/dL),Cre (mg/dL)

  8. kidney function 2 [3 months]

    eGFR (mL/min)

  9. kidney function 3 [3 months]

    Urine Albumin to Creatinine Ratio(mg/g)

  10. Gut microbiome [3 months]

    TMAO (uM)

  11. immune composition analysis 1 [3 months]

    CD3(%), CD4(%), CD8(%), CD56(%), CD11b(%), Foxp3(%), NK,HLA-DR(%)

  12. immune composition analysis 2 [3 months]

    WBC (10^3/uL)

  13. immune function analysis [3 months]

    IFN-gamma (IU/mL)

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • hypertension,

  • hyperlipidemia,

  • ischemic heart disease

  • diabetes

Exclusion Criteria:
  • cancer patients,

  • have comorbidities with poor control

  • patients with eGFR< 40 ml/min/1.73m2

  • who are pregnant, breastfeeding, and in their menstrual period when recruiting

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Buddhist Tzu Chi General Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Buddhist Tzu Chi General Hospital
ClinicalTrials.gov Identifier:
NCT05420987
Other Study ID Numbers:
  • IRB111-025-A
First Posted:
Jun 16, 2022
Last Update Posted:
Jun 16, 2022
Last Verified:
May 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Buddhist Tzu Chi General Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 16, 2022