EUCTR2006-000047-26-GBActive, not recruitingNot 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 enrollmentStarted: February 13, 2006Last updated:
Conditions
Drugs
Trial Snapshot
- Phase
- Not Applicable
- Status
- Active, not recruiting
- Sponsor
- Enrollment
- 44
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional clinical trial of medicinal product
Eligibility Criteria
- Sex
- All
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
Investigators
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