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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01958892
Other study ID # 2012/311/D
Secondary ID
Status Completed
Phase N/A
First received October 5, 2013
Last updated October 8, 2013

Study information

Verified date October 2013
Source Singapore General Hospital
Contact n/a
Is FDA regulated No
Health authority Singapore: Ministry of Health
Study type Observational

Clinical Trial Summary

The purpose of the study is to assess whether transurethral enucleation of prostate gives better or equivalent outcomes compared to the gold standard of transurethral resection of the prostate


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date
Est. primary completion date October 2012
Accepts healthy volunteers
Gender Male
Age group N/A and older
Eligibility Inclusion Criteria:

- All who underwent TURP or TUERP

Exclusion Criteria:

- Those with prostate cancer, neurogenic bladder, previous urethral or prostate surgery

Study Design

Observational Model: Cohort, Time Perspective: Retrospective


Intervention

Procedure:
TURP, TUERP


Locations

Country Name City State
Singapore Singapore General Hospital S'pore
Singapore Singapore General Hospital Singapore

Sponsors (1)

Lead Sponsor Collaborator
Singapore General Hospital

Country where clinical trial is conducted

Singapore, 

Outcome

Type Measure Description Time frame Safety issue
Primary Maximum urinary flow rate 6 weeks No
See also
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