Anticoagulant/Antiaggregant Use and Postoperative Bleeding Risk in Patients With Bladder Tumor and Benign Prostatic Hyperplasia
NCT ID: NCT05314582
Last Updated: 2023-07-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
500 participants
OBSERVATIONAL
2022-03-10
2023-01-10
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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TURP patients using anticoagulant/antiaggregant medication
Patients who used anticoagulant/antiaggregant medication for any reason (eg: coronary artery disease, atrial fibrillation, cerebrovascular disease) before surgery and underwent endoscopic prostatectomy (TURP).
No interventions assigned to this group
TURP patients not using anticoagulant/antiaggregant medication
Patients with no history of anticoagulant/antiaggregant medication and underwent endoscopic prostatectomy (TURP).
No interventions assigned to this group
TUR-BT patients using anticoagulant/antiaggregant medication
Patients who used anticoagulant/antiaggregant medication for any reason (eg: coronary artery disease, atrial fibrillation, cerebrovascular disease) before surgery and underwent endoscopic bladder tumor resection (TUR-BT).
No interventions assigned to this group
TUR-BT patients not using anticoagulant/antiaggregant medication
Patients with no history of anticoagulant/antiaggregant medication and underwent endoscopic bladder tumor resection (TUR-BT).
No interventions assigned to this group
Open prostatectomy patients using anticoagulant/antiaggregant medication
Patients who used anticoagulant/antiaggregant medication for any reason (eg: coronary artery disease, atrial fibrillation, cerebrovascular disease) before surgery and underwent open prostatectomy (OP).
No interventions assigned to this group
Open prostatectomy patients not using anticoagulant/antiaggregant medication
Patients with no history of anticoagulant/antiaggregant medication and underwent open prostatectomy (OP).
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Patients undergoing TURP due to benign prostatic hyperplasia
* Patients undergoing open prostatectomy due to benign prostatic hyperplasia
Exclusion Criteria
* Patient who underwent TUR biopsy for restaging with no obvious macroscopic tumoral lesion
* Patients who underwent cystectomy for bladder cancer
ALL
No
Sponsors
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Bezmialem Vakif University
OTHER
Responsible Party
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Abdullah İlktaç
Pincipal investigator
Principal Investigators
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Abdullah Ilktac, MD
Role: STUDY_CHAIR
Bezmialem Vakif University, Faculty of Medicine, Department of Urology
Locations
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Bezmialem Vakif University
Istanbul, , Turkey (Türkiye)
Countries
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Other Identifiers
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196083
Identifier Type: -
Identifier Source: org_study_id
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