Transient Urinary Incontinence After Holmium Laser Enucleation of the Prostate (HoLEP)
NCT ID: NCT01108367
Last Updated: 2011-05-10
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
204 participants
OBSERVATIONAL
2009-11-30
Brief Summary
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Because this problem is usually temporary, there has been little attempt at addressing the issue. Therefore, there has been no research devoted specifically to transient de novo UI associated with HoLEP.
1\. The aim of the present study was following:
1. to investigate the incidence of transient de novo UI after HoLEP for BPH
2. determine the predictors of early postoperative transient de novo UI.
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* presence of moderate or severe LUTS (International Prostate Symptom Score \[IPSS\] greater than 8)or maximum flow rate of less than 10 mL/s
Exclusion Criteria
* urethral stricture
* prostate carcinoma
* neurogenic bladder disease
50 Years
MALE
No
Sponsors
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Seoul National University Hospital
OTHER
Responsible Party
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Seoul National University Hospital
Principal Investigators
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Min Chul Cho, M.D.
Role: PRINCIPAL_INVESTIGATOR
Seoul National University Hospital
Jae-Seung Paick, M.D.,Ph.D.
Role: STUDY_CHAIR
Seoul National University Hospital
References
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Cho MC, Park JH, Jeong MS, Yi JS, Ku JH, Oh SJ, Kim SW, Paick JS. Predictor of de novo urinary incontinence following holmium laser enucleation of the prostate. Neurourol Urodyn. 2011 Sep;30(7):1343-9. doi: 10.1002/nau.21050. Epub 2011 Apr 28.
Other Identifiers
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HoLEPUI
Identifier Type: -
Identifier Source: org_study_id
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