Pain Relief - Tramadol Versus Ibuprofen

NCT00111046 · Status: UNKNOWN · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2005-11-10

No results posted yet for this study

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.

Conditions

  • Choroidal Melanoma
  • Melanoma
  • Eye Neoplasms

Interventions

DRUG

Ibuprofen

DRUG

Tramadol

Sponsors & Collaborators

  • Royal Liverpool University Hospital

    lead OTHER_GOV

Principal Investigators

  • Bertil Damato · Royal Liverpool University Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2001-02-28
Completion
2004-02-29

Countries

  • United Kingdom

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00111046 on ClinicalTrials.gov