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An Investigation Into the Prevalence, Cause and treatment of Unexplained Anamia in Diabetes - Anamia and Diabetes

An Investigation Into the Prevalence, Cause and treatment of Unexplained Anamia in Diabetes - Anamia and Diabetes

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2005-003057-28-GB
Enrollment
Unknown
Registered
2005-07-18
Start date
2005-08-25
Completion date
Unknown
Last updated
2012-03-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anaemia in Diabetes

Interventions

Trade Name: Neorecormon Product Name: Neorecormon Product Code: N/A Pharmaceutical Form: Injection* INN or Proposed INN: Erythropoietin Concentration unit: IU/l international unit(s)/litre Concentrati

Sponsors

University Hospital Aintree NHS Trust
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients must have diabetes mellitus Patients in active attendance at a designated care centre i.e. at least one visit in the last 6-12 months Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria: Patients aged <18years old Patients unwilling to participate in the study Patients with known cause of anaemia Patients with severe uncontrolled blood pressure Patients with evidence of cardiac decompensation

Design outcomes

Primary

MeasureTime frame
Main Objective: To determine the response of diabetic patients with anaemia of unknown origin to erythropoietin therapy;Secondary Objective: To determine the impact of anaemia and it's treatment on the patient's quality of life;Primary end point(s): Rise in Haemoglobin levels

Countries

United Kingdom

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026