Comparing Patient-adjusted Versus Physician-adjusted Titration of BIAsp 30 Combined With Metformin in Type 2 Diabetes Patients
This study is currently recruiting participants.
Verified May 2013 by Novo Nordisk
Sponsor:
Novo Nordisk
Information provided by (Responsible Party):
Novo Nordisk
ClinicalTrials.gov Identifier:
NCT01589653
First received: April 30, 2012
Last updated: May 16, 2013
Last verified: May 2013
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Purpose
This trial is conducted in Africa and Asia. The aim of this trial is to compare patient-adjusted versus physician-adjusted titration of BIAsp 30 combined with metformin in type 2 diabetes patients uncontrolled on NPH insulin.
| Condition | Intervention | Phase |
|---|---|---|
|
Diabetes Diabetes Mellitus, Type 2 |
Drug: biphasic insulin aspart 30 |
Phase 4 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | A 20-week Study Comparing Patient-adjusted Versus Physician-adjusted Titration of BIAsp 30 Combined With Metformin in Type 2 Diabetes Patients Uncontrolled on NPH Insulin |
Resource links provided by NLM:
Drug Information available for:
Metformin
Metformin hydrochloride
Insulin, NPH
Insulin human
Insulin aspart
U.S. FDA Resources
Further study details as provided by Novo Nordisk:
Primary Outcome Measures:
- Change in HbA1c from baseline [ Time Frame: Week 0, week 20 ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- Change in fasting plasma glucose (FPG) (laboratory values) from baseline [ Time Frame: Week 0, week 20 ] [ Designated as safety issue: No ]
- Number of hypoglycaemic episodes during the trial from baseline [ Time Frame: Week 20 ] [ Designated as safety issue: No ]
- Change in Patient Reported Outcomes: Treatment-Related Impact Measures for Diabetes (TRIM-D) [ Time Frame: Week 0, week 20 ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 180 |
| Study Start Date: | May 2012 |
| Estimated Study Completion Date: | January 2014 |
| Estimated Primary Completion Date: | January 2014 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Experimental: Subject-driven titration |
Drug: biphasic insulin aspart 30
Dose individually adjusted by the subjects themselves according to the titration algorithm every second week. Administered subcutaneously (s.c., under the skin) twice daily.
|
| Experimental: Investigator-driven titration |
Drug: biphasic insulin aspart 30
Dose individually adjusted according to the directions given by the investigator. Administered subcutaneously (s.c., under the skin) twice daily.
|
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Diagnosed with type 2 diabetes for a minimum of 12 months prior to screening
- Currently treated with a NPH insulin for at least 3 months prior to screening
- Stable treatment (no change in dose or regimen) with a total daily dose of at least 1500 mg metformin or maximum tolerated dose (minimum 1000 mg) ± additional OAD treatment.The metformin treatment must have been stable for at least 2 months prior to screening
- HbA1c between 7.0% and 10.0% (both inclusive). (One re-test within one week of screening visit is allowed. The last sample will be conclusive.)
- Body Mass Index (BMI) below or equal to 40.0 kg/m^2
- Able and willing to eat at least 2 main meals each day during the trial
- Able and willing to adhere to the protocol including compliance with performance of self measured plasma glucose (SMPG), injection regimen and titrating themselves according to the protocol
- Experience in performing self measured plasma glucose (SMPG)
Exclusion Criteria:
- Treatment with any thiazolidinedione (TZD) and Glucagon-like peptide-1 (GLP-1) receptor agonists or pramlintide within the last 3 months prior to screening
- Impaired hepatic function defined as alanine aminotransferase (ALAT) above or equal to 2.5 times upper referenced limit. (One re-test within one week of screening visit is allowed. The last sample will be conclusive.)
- Impaired kidney function with serum creatinine above or equal to 133 µmol/L (1.5 mg/dL) for males and above or equal to 124 µmol/L (1.4 mg/dL) for females. (One re-test within one week of screening visit is allowed. The last sample will be conclusive.)
- Cardiac problems or uncontrolled treated/untreated severe hypertension (defined as systolic blood pressure above or equal to 180 mmHg and/or diastolic blood pressure above or equal to 100 mmHg)
- Previous use of pre-mixed insulin products (pre-mixed insulin analogues or pre-mixed human preparations)
- Recurrent severe hypoglycaemia (more than 1 severe hypoglycaemic episode, during the last 12 months) or hypoglycaemic unawareness as judged by the Investigator or hospitalisation for diabetic ketoacidosis during the previous 6 months
- Known proliferative retinopathy or maculopathy requiring treatment
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01589653
Contacts
| Contact: Novo Nordisk | clinicaltrials@novonordisk.com |
Locations
| Indonesia | |
| Not yet recruiting | |
| Malang, Indonesia, 65111 | |
| Morocco | |
| Not yet recruiting | |
| Rabat, Morocco, 10000 | |
| Saudi Arabia | |
| Recruiting | |
| Jeddah, Saudi Arabia, 80215 | |
| Tunisia | |
| Recruiting | |
| Tunis, Tunisia, 1008 | |
Sponsors and Collaborators
Novo Nordisk
Investigators
| Study Director: | Sujoy Chowdhury | Novo Nordisk Pharma Gulf |
More Information
Additional Information:
No publications provided
| Responsible Party: | Novo Nordisk |
| ClinicalTrials.gov Identifier: | NCT01589653 History of Changes |
| Other Study ID Numbers: | BIASP-3968, U1111-1125-7572 |
| Study First Received: | April 30, 2012 |
| Last Updated: | May 16, 2013 |
| Health Authority: | Morocco: Ministry of Health Saudi Arabia: Ministry of Health Tunisia: Ministry of Public Health Indonesia: National Agency of Drug and Food Control |
Additional relevant MeSH terms:
|
Diabetes Mellitus Diabetes Mellitus, Type 2 Glucose Metabolism Disorders Metabolic Diseases Endocrine System Diseases Insulin aspart |
Insulin Metformin Insulin, NPH Hypoglycemic Agents Physiological Effects of Drugs Pharmacologic Actions |
ClinicalTrials.gov processed this record on May 16, 2013