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Effects of Pretreatment With Ibuprofen in Post-Electroconvulsive Therapy (ECT) Headache

Mental Disorders Clinical Trial

Official title:
Effects of Pretreatment With Ibuprofen in Post- ECT Headache

Clinical Trial Summary

The purpose of the study is to determine whether ibuprofen reduces post-ECT headache or reduces its severity.

Clinical Trial Description

The aim of the study is to compare the severity of headache between patients who are receiving ibuprofen prior to ECT treatment with patients receiving placebo prior to ECT treatment.

Patients will be randomly assigned to receive either 600 mg ibuprofen 90 min prior to treatment or placebo orally, blinded to patient, physician and treatment team.

Patients will be asked about their headache with a visual analogue scale (VAS) 2 hours prior to and within 2 hours after treatment, 2-month, 6- month and 1 year follow-up [5]. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00258791
Study type Interventional
Source Norwegian University of Science and Technology
Contact
Status Withdrawn
Phase N/A
Start date January 2012
Completion date May 2012
View Details
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