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Clinical Trials/ACTRN12607000102471
ACTRN12607000102471
Not yet recruiting
Not Applicable

A randomised study to investigate the effects of caudal lignocaine versus topical lignocaine on VAS pain scores in men undergoing trans-rectal ultrasound guided biopsy of the prostate for the detection of prostate cancer.

Dr Suzi Nou0 sites50 target enrollmentJanuary 31, 2007
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ConditionsProstate cancerCancer - Prostate

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Prostate cancer
Sponsor
Dr Suzi Nou
Enrollment
50
Status
Not yet recruiting
Last Updated
6 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
January 31, 2007
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
Male

Investigators

Sponsor
Dr Suzi Nou

Eligibility Criteria

Inclusion Criteria

  • •Inclusion: Adult patients undergoing TRUS biopsy of the prostate able to give consent.

Exclusion Criteria

  • •Allergy to lignocaine, known contraindication to neuraxial blockade (sepsis, abnormal spinal anatomy, bleeding diathesis)

Outcomes

Primary Outcomes

Not specified

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