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Completed

NCT Number: NCT00839878

A Survey to Evaluate Diabetes Management, Control, Chronic Complications, Psychosocial Aspects of Diabetic Subjects in Bangladesh

This study is conducted in Asia. The aim of this observational study is to evaluate current status of diabetes management, control, complications in diabetic subjects in Asia.

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Key information

Sex eligibility

All sexes

Study type

Observational

Primary location

Novo Nordisk Investigational Site

Dhaka, 1206, Bangladesh

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Diabetic patients registered in the particular centre for more than 12 months.
  • Patients should have visited the centre at least once in the last 3-6 months apart from the initial visit.
  • Patients willing to sign informed consent form.

Exclusion criteria

  • Repetition of any patient as patients should not be included twice for any reason.
  • Unwilling to participate or unable to comply with protocol requirements.

Treatment and study plan

No treatment given

Other

Subject will only fill out a questionaire when entering the observational study.

Primary outcomes

  1. Mean age of onset of type 1 and 2 diabetes mellitus

    Time frame: at baseline visit/study start

  2. Mean duration of treatment of type 2 DM

    Time frame: at baseline visit/study start

  3. Percentage of patients on Insulin and OAD therapy

    Time frame: at baseline visit/study start

  4. Mean duration of diabetes in type 1 and type 2 patients respectively

    Time frame: at baseline visit/study start

  5. Mean FPG and PPG of diabetic patients

    Time frame: at baseline visit/study start

  6. Mean HbA1c of diabetic patients

    Time frame: at baseline visit/study start

  7. Percentage of diabetic patients with HbA1c target below or equal to 7.0%.

    Time frame: at baseline visit/study start

  8. Percentage of diabetic patients with HbA1c target below or equal to 6.5%.

    Time frame: at baseline visit/study start

  9. Percentage of diabetic patients having dyslipidemia and hypertension

    Time frame: at baseline visit/study start

  10. Percentage of diabetic patients having cardiovascular complications

    Time frame: at baseline visit/study start

  11. Percentage of diabetic patients having peripheral vascular disease

    Time frame: at baseline visit/study start

  12. Percentage of diabetic patients having diabetic eye complications

    Time frame: at baseline visit/study start

  13. Percentage of diabetic patients having diabetic nephropathy

    Time frame: at baseline visit/study start

Secondary outcomes

  1. Patients' perception will be analysed through Patient questionnaire measuring:Psychological well-being, Quality of life and Patients' compliant to treatment

    Time frame: at baseline visit/study start

  2. Physician perception of diabetes and its management will be analysed through physician questionnaire measuring awareness about HbA1c test and its goal, anti-diabetic treatment and barriers towards optimum diabetes control

    Time frame: at baseline visit/study start

  3. Duration of diabetes associated with highest number of diabetic complications

    Time frame: at baseline visit/study start

  4. Minimum duration of diabetes associated with 10% incidence of diabetic complications (CVD, nephropathy and retinopathy)

    Time frame: at baseline visit/study start

Sponsors and collaborators

Lead sponsor

Novo Nordisk A/S

Industry

Registry information

Official study title

A Cross-Sectional Survey to Evaluate Diabetes Management, Control, Complications, Psychosocial Aspects of Diabetic Patients in Asia and To Evaluate Perceptions and Practices of Physicians and Patients About Diabetes Management in Asia DiabCare Asia 2008 (Bangladesh)

Acronym: DiabCare Asia

Important dates

Study start
2009
Primary completion
2009
Study completion
2009
First posted
Feb 10, 2009
Registry last updated
Oct 14, 2016

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.

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