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NCT00861367 Clinical Trial

Prospective Double-blind Study for the Use of Aspirin During Transurethral Surgery of the Bladder or the Prostate

Blood Loss, Surgical Clinical Trial

Official title:
Prospektive Doppel-Blind-randomisierte Studie Zur Verwendung Von Aspirin Bei Transurethralen Operationen

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT00861367
Other study ID # 05/08
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date September 2008
Est. completion date January 2009

Study information
Verified date March 2024
Source University Hospital, Basel, Switzerland
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Aspirin is very common in older patients. Therefore many of the investigators patients have aspirin. The aim of the study is to proof that Transurethral Surgery of the bladder or the prostate can be performed with aspirin.

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date January 2009
Est. primary completion date January 2009
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Transurethral surgery of the bladder or prostate, informed consent, age over 18 Exclusion Criteria: - Oral anticoagulation,

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• transurethral surgery with or without aspirin
aspirin 100mg once a day, transurethral surgery with or without aspirin

Locations
Country Name City State
Switzerland Urologische Universitätsklinik Basel-Liestal Liestal

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Basel, Switzerland

Country where clinical trial is conducted

Switzerland, 

Outcome
Type Measure Description Time frame Safety issue
Primary Blood loss intraoperative, 6 hours post op, 3 days postop
Secondary Reoperation rates during hospitalization
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