Skip to main content
Clinical Trials/EUCTR2006-000047-26-GB
EUCTR2006-000047-26-GB
Active, not recruiting
Not Applicable

A randomized controlled trial of caudal epidural or intravenous fentanyl on the post-operative analgesia requirements after transurethral endoscopic resection of prostate, bladder neck or bladder tumour. - Caudal epidural or iv fentanyl for transureth endoscopic analgesia

eeds Teaching Hospitals NHS Trust0 sites44 target enrollmentFebruary 13, 2006

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
eeds Teaching Hospitals NHS Trust
Enrollment
44
Status
Active, not recruiting
Last Updated
14 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
February 13, 2006
End Date
TBD
Last Updated
14 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
eeds Teaching Hospitals NHS Trust

Eligibility Criteria

Inclusion Criteria

  • Male and Female:
  • Aged over 18 years. There is no upper age limit.
  • Scheduled for bladder outlet surgery
  • Written informed consent
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1\.2 Adults (18\-64 years) yes
  • F.1\.2\.1 Number of subjects for this age range
  • F.1\.3 Elderly (\>\=65 years) yes
  • F.1\.3\.1 Number of subjects for this age range

Exclusion Criteria

  • INR \> 1\.5 on the day of surgery
  • Pregnant or lactating women\- a pregnancy test will be carried out if there is any risk of the patient being pregnant.
  • Platelet count \<80 on day of surgery
  • Current Clopidogrel treatment
  • On heparin, including high dose enoxaparin (\>40mg once daily)
  • Allergy or intolerance to local anaesthetics or fentanyl
  • Current administration of monamine oxidase inhibitors
  • Other contraindications to caudal epidural analgesia such as local sepsis

Outcomes

Primary Outcomes

Not specified

Similar Trials