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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04278495
Other study ID # LOSARTAN.OBST.UROPATHY
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 1, 2014
Est. completion date December 1, 2018

Study information

Verified date February 2020
Source Mansoura University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Previous experimental studies concluded that angiotensin receptor blockers can ameliorate the harmful inflammatory and histological changes after relief of obstruction. Nevertheless, these witnessed effects have not been yet translated into the clinical practice.


Recruitment information / eligibility

Status Completed
Enrollment 96
Est. completion date December 1, 2018
Est. primary completion date December 1, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- anuric and oliguric patients

- calculuar ureteral obstruction

Exclusion Criteria:

- anomalous kidney

- bilateral obstructed kidney

- history of recent use of angiotensin receptor blockers or angiotensin-converting enzyme inhibitors

- ASA score of >3

Study Design


Intervention

Drug:
Cozaar (Losartan Potassium 25mg)
Cozaar (Losartan Potassium 25mg)
Placebo
Placebo

Locations

Country Name City State
Egypt Urology and nephrology center Mansoura Outside U.S./Canada

Sponsors (1)

Lead Sponsor Collaborator
Mansoura University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Renographic glomerular filtration rate of the affected kidney. assessed by radioisotope renography using 99mTc-mercaptoacetyltriglycine (99mTc-MAG3) in ml/min 3 months
Secondary Serum creatinine change assessed by serum creatnine in mg/dl 3 months
See also
  Status Clinical Trial Phase
Recruiting NCT04384939 - Feasibility of Magnetic-end Double-J Ureteral Stent Use in Children N/A