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OpenTrials
Completed

NCT Number: NCT01958892

To Compare Outcomes After Transurethral Enucleation of Prostate Versus Transurethral Resection of Prostate

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

Completed

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Key information

Sex eligibility

Male

Study type

Observational

Primary location

Singapore General Hospital, S'pore, Singapore

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Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All who underwent TURP or TUERP

Exclusion criteria

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

Treatment and study plan

TURP, TUERP

Procedure

Primary outcomes

  1. Maximum urinary flow rate

    Time frame: 6 weeks

Sponsors and collaborators

Lead sponsor

Singapore General Hospital

Other

Registry information

Important dates

Primary completion
2012
First posted
Oct 9, 2013
Registry last updated
Oct 9, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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