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NCT00489723 Clinical Trial

Is There is a Role of Prophylactic Therapy With Tamsulosin Before Extracorporeal Shock Wave Lithotripsy to Avoid Development of Steinstrasse ?

Kidney Stones Clinical Trial

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT00489723
Other study ID # 0056-07-EMC
Secondary ID
Status Recruiting
Phase N/A
First received June 19, 2007
Last updated June 20, 2007
Start date May 2007

Study information
Verified date June 2007
Source HaEmek Medical Center, Israel
Contact DORON PEREZ, M.D.
Phone +972-4-6495115
Email perez_do@clalit.org.il
Is FDA regulated No
Health authority Israel: Ethics Commission
Study type Observational

Clinical Trial Summary

The purpose of this study is to determine if there is a role of prophylactic therapy with tamsulosin prior extracorporeal shock wave lithotripsy to avoid development of steinstrasse. 150 persons that will go to Extracorporeal shock wave lithotripsy will randomize to 2 groups.

Group 1 -of 75 persons will recieve tamsulosin 0.4 mg x 1/d 2 days before the lithotripsy .

Group 2 - of 75 persons will not recieve tamsulosin. 48 hour after the ESWL all 2 group will take abdominal radiograph to evaluate the presence of steinstrasse.

Recruitment information / eligibility
Status Recruiting
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender Both
Age group 15 Years to 85 Years
Eligibility Inclusion Criteria:

- size of stone 1-2 cm

Exclusion Criteria:

- ureteral stricture Presence of internal stent prior use of alfa bloker prior ESWL

Study Design

Observational Model: Defined Population, Primary Purpose: Screening, Time Perspective: Longitudinal

Related Conditions & MeSH terms

Intervention

Drug:
• tamsulosin 0.4mg

Locations
Country Name City State
Israel Haemek medical center Afula

Sponsors (1)
Lead Sponsor Collaborator
HaEmek Medical Center, Israel

Country where clinical trial is conducted

Israel, 

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