Overview

Pain Relief - Tramadol Versus Ibuprofen

Status:
Unknown status
Trial end date:
2004-02-01
Target enrollment:
0
Participant gender:
All
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.
Phase:
Phase 1/Phase 2
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Royal Liverpool University Hospital
Treatments:
Ibuprofen
Tramadol
Criteria
Inclusion Criteria:

- 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 Criteria:

- 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.