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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00140985
Other study ID # 0954-213
Secondary ID MK0954-2132005_0
Status Completed
Phase Phase 4
First received
Last updated
Start date February 2000
Est. completion date January 2002

Study information

Verified date February 2022
Source Organon and Co
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Antiproteinuric Efficacy of Losartan Potassium in Patients with Non-Diabetic Proteinuric Renal Diseases.


Recruitment information / eligibility

Status Completed
Enrollment 97
Est. completion date January 2002
Est. primary completion date January 2002
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Males or females at least 18 years of age with non-diabetic proteinuric renal diseases

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
MK0954, losartan potassium/Duration of Treatment: 20 weeks

Comparator: amlodipine / Duration of Treatment: 20 weeks


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Organon and Co

References & Publications (1)

Praga M, Andrade CF, Luño J, Arias M, Poveda R, Mora J, Prat MV, Rivera F, Galceran JM, Ara JM, Aguirre R, Bernis C, Marín R, Campistol JM. Antiproteinuric efficacy of losartan in comparison with amlodipine in non-diabetic proteinuric renal diseases: a do — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary 24h proteinuria
Secondary Changes in the plasma and urinary levels of TGF-beta
See also
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