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.
Investigators
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
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