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Comparison of the Blood Sugar Lowering Effect Between Repaglinide Plus Metformin and Repaglinide Alone in Type 2 Diabetics Not Previously Treated With Oral Sugar-lowering Drugs

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00819741
First Posted: January 9, 2009
Last Update Posted: February 10, 2017
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Novo Nordisk A/S
  Purpose
This trial is conducted in Asia. The aim of this clinical trial is to investigate the blood sugar lowering effect of repaglinide plus metformin as initial treatment compared to repaglinide alone in Chinese subjects with type 2 diabetes having an HbA1c (glycosylated haemoglobin A1c) over 8.5 % and who never have taken oral sugar-lowering drugs before. The associated unfavourable events including low blood sugar episodes between the two treatments are also compared.

Condition Intervention Phase
Diabetes Diabetes Mellitus, Type 2 Drug: repaglinide Drug: metformin Phase 4

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A 16-week, Open-label, Multicentre, Randomised, Parallel Study to Evaluate Efficacy and Safety of Repaglinide and Metformin Combination Therapy Compared to Repaglinide Monotherapy in Chinese OAD Naive Type 2 Diabetic Patients

Resource links provided by NLM:


Further study details as provided by Novo Nordisk A/S:

Primary Outcome Measures:
  • Change in Glycosylated Haemoglobin A1c (HbA1c) [ Time Frame: week -2 (screening), week 16 ]
    Calculated as an estimate of the mean change in HbA1c after 16 weeks of treatment.


Secondary Outcome Measures:
  • Change in Fasting Plasma Glucose [ Time Frame: week 0, week 16 ]
    Calculated as an estimate of the mean change in fasting plasma glucose after 16 weeks of treatment.

  • Change in 2-hour Postprandial Plasma Glucose [ Time Frame: Week 0, week 16 ]
    Calculated as an estimate of the mean change in 2-hour postprandial plasma glucose following a standard test meal after 16 weeks of treatment

  • Change in 7-point Plasma Glucose Profile [ Time Frame: Week 0, week 16 ]
    Calculated as an estimate of the mean change in 7-point (before breakfast, 2 hours after breakfast, before lunch, 2 hours after lunch, before dinner, 2 hours after dinner, bedtime) plasma glucose profile after 16 weeks of treatment.

  • Change in Fasting Serum Insulin [ Time Frame: Week 0, week 16 ]
    Calculated as an estimate of the mean change in fasting serum insulin after 16 weeks of treatment.

  • Change in 2-hour Postprandial Serum Insulin [ Time Frame: Week 0, week 16 ]
    Calculated as an estimate of the mean change in 2-hour postprandial serum insulin after 16 weeks of treatment.

  • Change in Fasting Serum C-peptide [ Time Frame: Week 0, week 16 ]
    Calculated as an estimate of the mean change in fasting serum C-peptide after 16 weeks of treatment

  • Change in 2-hour Postprandial Serum C-peptide [ Time Frame: Week 0, week 16 ]
    Calculated as an estimate of the mean change in 2-hour postprandial serum C-peptide after 16 weeks of treatment

  • Hypoglycaemic Episodes [ Time Frame: Weeks 0-16 ]
    Number of hypoglycaemic episodes from Week 0 to Week 16, defined as major, minor or symptoms only. Major if unable to treat her/himself. Minor if able to treat her/himself and plasma glucose below 3.1 mmol/L. Symptoms only if able to treat her/himself and no plasma glucose measurement or plasma glucose higher than or equal to 3.1 mmol/L.

  • Change in Blood Pressure [ Time Frame: Week 0, week 16 ]
    Calculated as the mean change in diastolic and systolic blood pressure after 16 weeks of treatment

  • Physical Examinations [ Time Frame: Week -2, week 16 ]
    The number of subjects having a physical examination event that changed from 'Normal' or 'Abnormal, not clinically significant' to 'Abnormal, clinically significant'. Physical examination included cardiovascular system, respiratory system, musculoskeletal system, nervous system and abdomen.

  • ECG (ElectroCardioGram) [ Time Frame: Week -2, week 16 ]
    The number of subjects having a electrocardiogram (ECG) that changed from 'Normal' or 'Abnormal, not clinically significant' to 'Abnormal, clinically significant'. 'Abnormal, Clinically significant' is an abnormality that suggests a disease and/or organ toxicity and is of a severity, which requires active management.

  • Biochemistry: Alanine Aminotransferase (ALAT) [ Time Frame: Week -2, week 16 ]
    The number of subjects having a change in Alanine Aminotransferase (ALAT) from 'Normal' or 'Abnormal, not clinically significant' to 'Abnormal, clinically significant'. 'Abnormal, Clinically significant' is an abnormality that suggests a disease and/or organ toxicity and is of a severity, which requires active management.

  • Biochemistry: Alanine Aminotransferase (ASAT) [ Time Frame: Week -2, week 16 ]
    The number of subjects having a change in Aspartate Aminotransferase (ASAT) from 'Normal' or 'Abnormal, not clinically significant' to 'Abnormal, clinically significant'. 'Abnormal, Clinically significant' is an abnormality that suggests a disease and/or organ toxicity and is of a severity, which requires active management.

  • Haematology: Haemoglobin [ Time Frame: Week -2, week 16 ]
    Haemoglobin was measured. The number of subjects having a change in Haemoglobin measurement from 'Normal' or 'Abnormal, not clinically significant' to 'Abnormal, clinically significant' 'Abnormal, Clinically significant' is an abnormality that suggests a disease and/or organ toxicity and is of a severity, which requires active management.


Enrollment: 433
Study Start Date: February 2009
Study Completion Date: November 2009
Primary Completion Date: November 2009 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Repaglinide + metformin
Initial dose of repaglinide 1mg plus metformin 500mg once daily. During the dose titration period of 6 weeks, the dose could be titrated up to repaglinide 4 mg and metformin 500 mg three times daily, according to fasting glucose values. The minimal dose was repaglinide 1 mg plus metformin 500 mg three times daily.
Drug: repaglinide
The dose was started from repaglinide 1 mg plus metformin 500 mg once daily. During the dose titration period, the dose could be titrated up to repaglinide 4 mg and metformin 500mg three times daily, according to fasting glucose. the minimal dose was repaglinide 1 mg plus metformin 500 mg three times daily
Drug: metformin
The dose was started from repaglinide 1 mg plus metformin 500 mg once daily. During the dose titration period, the dose could be titrated up to repaglinide 4 mg and metformin 500 mg three times daily, according to fasting glucose. the minimal dose was repaglinide 1 mg plus metformin 500 mg three times daily
Active Comparator: Repaglinide
Initial dose of repaglinide 1 mg three times daily. During the dose titration period of 6 weeks, the dose of repaglinide could be titrated up to 4 mg three times daily, according to fasting glucose values. The minimal dose was repaglinide 1 mg three times daily.
Drug: repaglinide
The dose was started from repaglinide 1 mg three times daily. During the dose titration period, the dose of repaglinide could be titrated up to 4 mg three times daily, according to fasting glucose.

  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   18 Years to 75 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Diagnosed with type 2 diabetes
  • Never taken oral antidiabetic drugs before
  • HbA1c greater than 8.5 %
  • BMI (Body Mass Index) less than or equal to 35 kg/m^2

Exclusion Criteria:

  • Known or suspected allergy to repaglinide, metformin, or any of the excipients in the medications
  • Taken an investigational drug in another clinical trial within 4 weeks prior to this trial
  • Impaired liver function, defined as ASAT (aspartate aminotransferase) or ALAT (alanine aminotransferase) equal to or greater than 2 times upper normal limit
  • Have a clinically significant, active disease of the gastrointestinal, pulmonary, neurological, renal, genitourinary, and haematological systems
  • Severe uncontrolled or untreated hypertension (sitting diastolic blood pressure (BP) equal to or greater than 100 mmHg or systolic BP equal to or greater than 180 mmHg)
  • Impaired renal function
  • Acute or chronic acidosis or if there are plans to have a radiographic material containing iodine
  • Have a clinically significant, active cardiovascular disease, or decompensated heart failure
  • Treatment with systemic corticosteroids within the past two months prior to screening
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00819741


Locations
China, Fujian
Novo Nordisk Investigational Site
Fuzhou, Fujian, China, 350001
China, Jiangsu
Novo Nordisk Investigational Site
Nanjing, Jiangsu, China, 210009
Novo Nordisk Investigational Site
Nanjing, Jiangsu, China, 210012
Novo Nordisk Investigational Site
Nanjing, Jiangsu, China, 210029
Novo Nordisk Investigational Site
Suzhou, Jiangsu, China, 215004
Novo Nordisk Investigational Site
Wuxi, Jiangsu, China, 214023
China, Jiangxi
Novo Nordisk Investigational Site
Nanchang, Jiangxi, China, 330006
China, Shanghai
Novo Nordisk Investigational Site
Shanghai, Shanghai, China, 200001
Novo Nordisk Investigational Site
Shanghai, Shanghai, China, 200025
Novo Nordisk Investigational Site
Shanghai, Shanghai, China, 200072
Novo Nordisk Investigational Site
Shanghai, Shanghai, China, 200092
Novo Nordisk Investigational Site
Shanghai, Shanghai, China, 200120
China, Zhejiang
Novo Nordisk Investigational Site
Hangzhou, Zhejiang, China, 310003
Novo Nordisk Investigational Site
Wenzhou, Zhejiang, China, 325000
China
Novo Nordisk Investigational Site
Hangzhou, China, 310016
Novo Nordisk Investigational Site
Nantong, China, 226001
Novo Nordisk Investigational Site
Shanghai, China, 200040
Sponsors and Collaborators
Novo Nordisk A/S
Investigators
Study Director: Global Clinical Registry (GCR, 1452) Novo Nordisk A/S
  More Information

Additional Information:
Publications:
Responsible Party: Novo Nordisk A/S
ClinicalTrials.gov Identifier: NCT00819741     History of Changes
Other Study ID Numbers: AGEE-3705
First Submitted: January 8, 2009
First Posted: January 9, 2009
Results First Submitted: November 5, 2010
Results First Posted: December 8, 2010
Last Update Posted: February 10, 2017
Last Verified: December 2016

Additional relevant MeSH terms:
Diabetes Mellitus
Diabetes Mellitus, Type 2
Glucose Metabolism Disorders
Metabolic Diseases
Endocrine System Diseases
Repaglinide
Metformin
Hypoglycemic Agents
Physiological Effects of Drugs