A Test of the Comparison Between Trans-rectal and Trans-perineal Biopsy of Prostate

Status

UNKNOWN

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT01849835

Acronym

RCT

Enrollment

120

Registered

2013-05-09

Start date

2013-01-31

Completion date

Unknown

Last updated

2014-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Complication

Keywords

rate of positive detection

Brief summary

The purpose of this randomized controlled trial (RCT) is to compare the two ways (tras-rectal and trans-perineal) to perform prostate biopsy from the rate of Positive detection, complications, pain level, operation time and costs et al.

Interventions

PROCEDUREtrans-rectal to perform the prostate biopsy

the puncture points are at the rectal

PROCEDUREtrans-perineal to perform the prostate biopsy

the puncture points are at the perineal

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

DIAGNOSTIC

Masking

NONE

Eligibility

Sex/Gender

MALE

Age

No minimum to 80 Years

Healthy volunteers

Inclusion criteria

* prostate-specific antigen \> 4ng/ml * Palpation is positive

Exclusion criteria

* older than 80y * prostate-specific antigen \> 100 ng/ml

Design outcomes

Primary

Measure	Time frame
the rate of positive detections	1year

Secondary

Measure	Time frame
the incidence rate of each complication	1 year

Other

Measure	Time frame
pain level assessed by visual analogue scale	1 year

Countries

China

Contacts

Primary Contactguo lehang, phd

gopp1314@hotmail.com+8613764538305

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026