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CHM for T2DM & MetS

H

Hong Kong Baptist University

Status

Not yet enrolling

Conditions

Type 2 Diabetes Mellitus With Metabolic Syndrome

Treatments

Drug: Chinese Herbal Medicine granules

Study type

Interventional

Funder types

Other

Identifiers

NCT06450652
REC/23-24/0397

Details and patient eligibility

About

This is a single-arm design. A total of 15 Type 2 Diabetes Mellitus (T2DM) patients with comorbid Metabolic Syndrome (MetS) will be recruited from community. The intervention will be a 4-week of Chinese Herbal Medicine granules treatment, which will consist of six Chinese herbs. The primary outcome measure will be fasting plasma glucose and blood pressure. Secondary outcome measures including changes of anthropometric data (body mass index, waist-to-hip ratio), lipid panels (total cholesterol, triglycerides, high-density lipoprotein, low-density lipoprotein), HbA1C, Framingham Stroke Risk Score (FSRS), Audit of diabetes-dependent quality of Life (ADDQoL), International Physical Activity Questionnaire Short Form (IPAQ-SF), daily step count and physiological parameters from wearable watch, dietary record, retinal and sublingual vein imaging, concurrent medications and adverse events.

Enrollment

15 estimated patients

Sex

All

Ages

30 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age between 30-75y.
  • Diagnosed with Type 2 diabetes no more than 5 years.
  • Having current prehypertension (systolic blood pressure 130-139 mmHg or diastolic blood pressure 85-89mmHg), or with a history of hypertension (systolic blood pressure 140-159mmHg or diastolic blood pressure 90-99mmHg).
  • Diagnosed with Metabolic Syndrome according to Guideline for the prevention and treatment of type 2 diabetes mellitus in China (2020 edition) from Chinese Diabetes Society. People who meet 3 of the following diagnostic criteria or more can be diagnosed as Metabolic Syndrome: (a)Abdominal obesity: waist circumference ≥ 90cm for male and ≥ 85cm for female; (b) Hyperglycemia: Fasting blood glucose ≥ 6.1mmol/L or 2-hour postprandial glucose ≥ 7.8mmol/L and/or those who have been diagnosed with hyperglycemia and in treatment; (c) Hypertension: blood pressure ≥ 130/85mmHg and/or those who have been diagnosed with hypertension and in treatment; (d) Fasting triglyceride ≥ 1.70mmol/L; (e) Fasting HDL-C < 1.04mmol/L.
  • Diagnosed with Accumulation of phlegm and dampness pattern or Intertwined phlegm and blood stasis pattern based on Traditional Chinese Medicine (TCM) theory.
  • Stable vital signs and with sufficient sensorimotor and language competency for completing assessments.

Exclusion criteria

  • Allergic history to Chinese herbal drugs or a known allergy to the ingredients of the CHM.
  • Diagnosed with type 1 diabetes, steroid-induced diabetes, gestational diabetes, or specific types of diabetes.
  • Diabetes accompanied by severe complications such as diabetic nephropathy, diabetic ketoacidosis, etc.
  • Secondary obesity (e.g., secondary to pituitary inflammation, tumor, etc.).
  • Secondary hypertension (e.g., pheochromocytoma, renal hypertension, etc.).
  • Secondary hyperlipidemia (e.g., hypothyroidism, nephrotic syndrome, etc.).
  • Experienced at least one day of diarrhea in the past 7 days.
  • With previous stroke history.
  • With unconsciousness, aphasia, and cognitive dysfunction.
  • With severe heart, liver, or kidney disease or bleeding disorders, or with other serious diseases (e.g. cancer, dementia, etc.).
  • Pregnancy or lactation female.
  • Had joined other clinical trial within past 4 weeks.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

15 participants in 1 patient group

Chinese Herbal Medicine granules
Experimental group
Treatment:
Drug: Chinese Herbal Medicine granules

Trial contacts and locations

0

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Central trial contact

Jialing ZHANG, PhD

Data sourced from clinicaltrials.gov

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