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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02444845
Other study ID # ML27762
Secondary ID
Status Completed
Phase
First received May 12, 2015
Last updated March 19, 2018
Start date May 2011
Est. completion date August 2012

Study information

Verified date March 2018
Source Hoffmann-La Roche
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to evaluate the prevalence of CKD-related anemia at an early stage through screening of high-risk patients in Pakistan at the level of physicians, cardiologists, and diabetologists. The information gathered may serve as a foundation in formulating national guidelines for better early diagnosis and management of patients with CKD.


Recruitment information / eligibility

Status Completed
Enrollment 246
Est. completion date August 2012
Est. primary completion date August 2012
Accepts healthy volunteers No
Gender All
Age group 40 Years and older
Eligibility Inclusion Criteria:

- Age greater than or equal to 40 years

- Known hypertension and/or diabetes for at least 3 years

- Positive dipstick test result for proteinuria

Exclusion Criteria:

- Known CKD

- Receiving erythropoietin

- Blood transfusion within 8 weeks

- History of acute or chronic bleeding, hemolysis, or hemoglobinopathy

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Hoffmann-La Roche

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of patients with anemia secondary to CKD Up to 12 months
Secondary Use of treatment modalities for the management of anemia secondary to CKD Up to 12 months