Status:
UNKNOWN
Pain Relief - Tramadol Versus Ibuprofen
Lead Sponsor:
Royal Liverpool University Hospital
Conditions:
Choroidal Melanoma
Melanoma
Eligibility:
All Genders
18+ years
Phase:
PHASE1
PHASE2
Brief Summary
The purpose of this study is to assess post operative pain following the insertion of radioactive plaque for choroidal melanoma in patients after receiving either ibuprofen or tramadol.
Detailed Description
Patients with choroidal melanomas who are offered ruthenium plaque radiotherapy have their plaque sutured to the sclera under general anaesthesia. The plaque is removed in a few days after delivering ...
Eligibility Criteria
Inclusion
- All patients that are admitted for undergoing plaque radiotherapy for choroidal melanoma would be approached to participate in this study.
- They should be adults who are of a sound frame of mind to give an informed consent to participate.
Exclusion
- Patients less than 18 years of age
- Patients of unsound mind not capable of giving informed consent
- Active peptic ulcer disease, asthma, renal dysfunction, warfarin therapy, hypothyroidism history of epilepsy, pregnancy, breastfeeding and hypersensitivity to either products.
Key Trial Info
Start Date :
February 1 2001
Trial Type :
INTERVENTIONAL
End Date :
February 1 2004
Estimated Enrollment :
40 Patients enrolled
Trial Details
Trial ID
NCT00111046
Start Date
February 1 2001
End Date
February 1 2004
Last Update
November 10 2005
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
Royal Liverpool University Hospital
Liverpool, Merseyside, United Kingdom, L8 0RU