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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT00258791
Other study ID # LVS-2005
Secondary ID
Status Withdrawn
Phase N/A
First received November 24, 2005
Last updated September 21, 2012
Start date January 2012
Est. completion date May 2012

Study information

Verified date September 2012
Source Norwegian University of Science and Technology
Contact n/a
Is FDA regulated No
Health authority Norway: Norwegian Social Science Data Services
Study type Interventional

Clinical Trial Summary

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


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].


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date May 2012
Est. primary completion date May 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients receiving ECT

Exclusion Criteria:

- Pregnancy, contraindications to ibuprofen

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


Intervention

Drug:
Ibuprofen


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Norwegian University of Science and Technology
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