Mental Disorders Clinical Trial
Official title:
Effects of Pretreatment With Ibuprofen in Post- ECT Headache
The purpose of the study is to determine whether ibuprofen reduces post-ECT headache or reduces its severity.
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].
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment
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