Impact of Anticoagulants and Antiplatelets in Patients on Transurethral Resection of the Prostate
NCT ID: NCT02822963
Last Updated: 2020-10-06
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
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
WITHDRAWN
OBSERVATIONAL
2016-03-31
2016-08-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Anticoagulant/Antiaggregant Use and Postoperative Bleeding Risk in Patients With Bladder Tumor and Benign Prostatic Hyperplasia
NCT05314582
Transthoracic Echocardiographic Evaluation of the Cardiac Function During Transurethral Resection of Prostate in Elderly Patients
NCT02288780
The Risk Factor and Outcome of Transient Incontinence After Prostate Enucleation Surgery
NCT05116592
Prostate Artery Embolization for Symptomatic Benign Prostatic Hyperplasia
NCT02822924
Transurethral Ventral Wall of Urethra-preserving Enucleation of Prostate
NCT01073241
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
A
Non anticoagulant and/or antiplatelet users.
No interventions assigned to this group
B
Anticoagulant and/or antiplatelet users that hold their drugs during perioperative periods.
No interventions assigned to this group
C
Anticoagulant and/or antiplatelet users that doesn't hold their drugs during perioperative periods.
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Older than 20 years old
* Agree to participate this study
* Receiving transurethral resection of the prostate for benign prostatic hyperplasia or prostate cancer
Exclusion Criteria
20 Years
MALE
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
National Cheng-Kung University Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
National Cheng Kung University Hospital
Tainan City, , Taiwan
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
A-ER-105-045
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.