Diabetes Mellitus, Type 2 Clinical Trial
Official title:
An International Survey on Hypoglycaemia Among Insulin-treated Patients With Diabetes
Verified date | March 2019 |
Source | Novo Nordisk A/S |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
This study is conducted globally. The aim of this study is to describe the proportion of patients with hypoglycaemic episodes and estimate the incidence of various types of hypoglycaemia in the retrospective and prospective periods.
Status | Completed |
Enrollment | 7315 |
Est. completion date | May 14, 2015 |
Est. primary completion date | May 14, 2015 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - Informed consent obtained before any trial-related activities - Patient with T1DM or T2DM treated with insulin for more than 12 months - Male or female patient at least 18 years of age at the time of inclusion in the study Exclusion Criteria: - Previous participation in this study - Mental incapacity, unwillingness or language barriers precluding adequate understanding or cooperation - Illiterate patients and patients otherwise unable to sign the Informed Consent or complete a written survey - Non-ambulatory patients - Simultaneous participation in any other clinical study with an investigational product |
Country | Name | City | State |
---|---|---|---|
Bangladesh | Novo Nordisk Investigational Site | Dhaka | |
Colombia | Novo Nordisk Investigational Site | Bogotá | |
Egypt | Novo Nordisk Investigational Site | Cairo | |
Philippines | Novo Nordisk Investigational Site | Manilla | |
Singapore | Novo Nordisk Investigational Site | Singapore | |
South Africa | Novo Nordisk Investigational Site | Pretoria | |
Turkey | Novo Nordisk Investigational Site | Ankara | |
United Arab Emirates | Novo Nordisk Investigational Site | Ajman |
Lead Sponsor | Collaborator |
---|---|
Novo Nordisk A/S |
Bangladesh, Colombia, Egypt, Philippines, Singapore, South Africa, Turkey, United Arab Emirates,
Emral R, Pathan F, Cortés CAY, El-Hefnawy MH, Goh SY, Gómez AM, Murphy A, Abusnana S, Rudijanto A, Jain A, Ma Z, Mirasol R; IO HAT Investigator Group. Self-reported hypoglycemia in insulin-treated patients with diabetes: Results from an international surv — View Citation
Emral R, Tetiker T, Sahin I, Sari R, Kaya A, Yetkin I, Cil SU, Tütüncü NB; IO HAT investigator group. An international survey on hypoglycemia among insulin-treated type I and type II diabetes patients: Turkey cohort of the non-interventional IO HAT study. — View Citation
Faruque Pathan, Su-Yen Goh, Achmad Rudijanto, Arvind Gadekar, Anand Jain, Nemencio Nicodemus Jr. Hypoglycaemia among Insulin-Treated Patients with Diabetes: Southeast Asia Cohort of IO HAT Study Journal of the ASEAN Federation of Endocrine Societies
Pathan MF, Fariduddin M, Nazimuddin K, Mollah AS, Islam Siddiqui MN, Hassan KA, Ferdous HS, Rahman MH, Ashrafuzzaman SM, Sobhan MJ, E-Tanvir Haider MR, Amin MF. The Incidence of Hypoglycemia among Insulin-Treated Patients with Type 1 or Type 2 Diabetes: B — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The percentage of patients who experience at least 1 hypoglycaemic episode | During the 4-week prospective observational period | ||
Secondary | Incidence of any hypoglycaemic episodes | In the 4 weeks before and 4 weeks after the baseline (day 1) | ||
Secondary | Incidence of hypoglycaemic episodes requiring hospital admission | In the 6 months before and 4 weeks after the baseline (day 1) | ||
Secondary | Incidence of severe hypoglycaemic episodes | In the 6 months before and 4 weeks after the baseline (day 1) | ||
Secondary | Incidence of non-severe hypoglycaemic episodes | In the 4 weeks before and 4 weeks after the baseline (day 1) | ||
Secondary | Incidence of documented symptomatic hypoglycaemic episodes | In the 4 weeks after the baseline visit (day 1) | ||
Secondary | Incidence of all hypoglycaemic episodes associated with a blood glucose measurement below 3.1 mmol/L (56 mg/dl) irrespective of symptoms | In the 4 weeks following the baseline visit (day 1) | ||
Secondary | Incidence of hypoglycaemic episodes | Between midnight and 6 a.m. in the 4 weeks before and 4 weeks after the baseline visit (day 1) | ||
Secondary | Incidence of probable symptomatic hypoglycaemia | In the 4 weeks following the baseline visit (day 1) | ||
Secondary | Frequency of blood glucose monitoring | Over 1 day | ||
Secondary | Patient reported fear of hypoglycaemia | Over one day | ||
Secondary | Patient reported recovery times | One day | ||
Secondary | Proportion of patients consulting a doctor | Over one day | ||
Secondary | Proportion of patients increasing calorie intake | Over one day | ||
Secondary | Proportion of patients avoiding physical exercise | Over one day | ||
Secondary | Proportion of patients reducing or skipping insulin dose | Over one day | ||
Secondary | Proportion of patients increasing the number of blood glucose monitoring as a result of fear of hypoglycaemia or hypoglycaemic episodes | Over one day | ||
Secondary | Proportion of patients taking any sick leave, sick days or short days as a result of hypoglycaemic episodes | Over one day | ||
Secondary | DSQOLS (Diabetes-Specific Quality-of-Life Scale) scores | Over last 4 weeks |
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