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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01615315
Other study ID # SNUBH-URO-2012-01
Secondary ID
Status Completed
Phase N/A
First received June 6, 2012
Last updated August 27, 2012
Start date August 2012

Study information

Verified date August 2012
Source Seoul National University Hospital
Contact n/a
Is FDA regulated No
Health authority Korea: Institutional Review Board
Study type Observational

Clinical Trial Summary

Aspirin can increase the risk of bleeding tendency. However, correlation between aspirin treatment and hematuria in general population is not well known. The investigators will evaluate whether daily use of aspirin increase the risk of microscopic hematuria in healthy large screened populations.


Recruitment information / eligibility

Status Completed
Enrollment 60048
Est. completion date
Est. primary completion date August 2012
Accepts healthy volunteers No
Gender Both
Age group 20 Years to 89 Years
Eligibility Inclusion Criteria:

- Age = 20 years, male or female

Exclusion Criteria:

- No result of urinalysis

- No record of medical history (including medication)

Study Design

Observational Model: Cohort, Time Perspective: Retrospective


Locations

Country Name City State
Korea, Republic of Seoul National University Bundang Hospital Seongnam Gyeonggi-do

Sponsors (2)

Lead Sponsor Collaborator
Seoul National University Hospital Seoul National University Bundang Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence rate of the microscopic hematuria >4 RBC/HPF in urine microscopy at the screening No
Secondary Detection rate of significant cause for microscopic hematuria Among participants who had microscopic hematuria at the screening
By imaging study or cystoscopy
At the screening or within 12 months after screening
Significant cause for microscopic hematuria
urinary stone
renal mass (benign or malignant / not simple cyst)
urothelial cancer
other lesions (clinically relevant lesions determined by researchers)
whitin 12 months after screening No
Secondary Incidence rate of persistent microscopic hematuria Among participants who had microscopic hematuria at the screening
Determined by repeated urine microscopy
within 12 months No
See also
  Status Clinical Trial Phase
Terminated NCT02213757 - Effect of Vaginal Estrogen on Asymptomatic Microhematuria (AMH) Phase 4