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NCT Number: NCT02161276

Clinical Trials for the Optimal Dosage of Tang Ning Tongluo Capsule

Treatment of diabetes mellitus with Traditional Chinese Medicine has a long history.

aim: --establish the optimal dosage of traditional Chinese medicine Tang Ning Tongluo Capsule to treat type II diabetes mellitus.

---Preliminary evaluate the clinical efficacy and safety of Tangning Tongluo Capsule in the treatment of type II diabetes

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

Tianyuan Hospital of Guiyang City

Guiyang, Guizhou, 550007, China

About this study

Preliminary evaluation on the clinical efficacy and safety of Tangning Tongluo Capsule in the treatment of type II diabetes, and provides basis for determining optimal dosage of Tangning Tongluo capsule.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Fulfilled diagnostic criteria for type II diabetes and TCM syndrome diagnostic criteria.
  • Age between 18-70 years.
  • The blood sugar meet the following criteria: fasting blood glucose ≥ 7.0mmol/L, ≤ 13 mmol/L and (or) ≥ 2 hour postprandial blood glucose 11.1 mmol/L, ≤ 16 mmol/L; eligible conditions in blood glucose, glycosylated hemoglobin to ≤ 10%.
  • Traditional Chinese medicine symptom score ≥ 4 points.
  • Participated in the experiment voluntarily, and signed the informed consent form.

Exclusion criteria

  • Durring the cleaning period, blood sugar dropped to below detection diagnosis value through diet, increasing activity.
  • Secondary diabetes mellitus or nearly a month using insulin; or is the use of insulin sensitizers (thiazolidine two ketones), repaglinide, Bernard Glenn Nai, alpha glucoside enzyme inhibitor (acarbose, voglibose), other traditional Chinese medicine.
  • Within the past 1 months, with diabetic ketoacidosis and other acute metabolic disorders.
  • ALT is 2 times higher than the upper limit of the normal value, Cr is higher than the upper limit of normal persons.
  • Has severe heart, liver, renal, hematopoietic system disease, or other serious diseases and mental disease patients.
  • Pregnant, lactating women and prepare for pregnancy.
  • The allergic constitution and the drug allergy known composition.
  • For nearly a month with severe infection or other emergency state, such as trauma, operation etc..
  • within the past 3 months, participated in the other drugs.

Treatment and study plan

TNTL capsule

Drug

Patients were asked to taken drugs 3 times a day, with each time 3 grains

Other names: Tang Ning Tongluo Capsule

Placebo

Drug

Patients were asked to taken drugs 3 times a day, with each time 3 grains

Primary outcomes

  1. The decline glycosylated hemoglobin A1C and blood glucose level

    Time frame: up to 8 weeks

    Decline in Hemoglobin A1C and blood glucose level

Secondary outcomes

  1. The clinical composite safety evaluation of Tangning Tongluo Capsule in the treatment of type II diabetes participants

    Time frame: 2 months

    Routine check for blood, urine, stool + occult blood, liver function (ALT, AST, AKP, GGT, TBIL), renal function (BuN, Cr), ECG before treatment with 1 times per week.

Sponsors and collaborators

Lead sponsor

Guizhou Bailing Group Pharmaceutical Co Ltd

Industry

Collaborators

  • China-Japan Friendship Hospital

Registry information

Official study title

Phase 2 Study of The Optimal Dosage of Tang Ning Tongluo Capsule for Type II Diabetes

Acronym: TNTL

Important dates

Study start
2014
Primary completion
2014
Study completion
2014
First posted
Jun 11, 2014
Registry last updated
Sep 11, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.