Intravenous Haloperidol efficacy in improving conversion disorder patients in emergency
Not Applicable
- Conditions
- conversion disorder.Dissociative [conversion] disorders
- Registration Number
- IRCT201108317449N1
- Lead Sponsor
- Shahid Beheshti Medical University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 168
Inclusion Criteria
All patients with conversion disorder according to DSM IV criteria referred to emergency room.
Exclusion criteria: Patients with abnormal vital signs; ill; under 18; over 60; pregnant patients; opium addicted patients; Unwillingness to cooperation
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The patient feel better. Timepoint: Before the intervention, one hour after the intervention and one week after intervention. Method of measurement: Standardized questionnaire, the patients feel better, better expressed by the patient and his companions.;The patient's symptoms disappear. Timepoint: Before the intervention, one hour after the intervention and one week after intervention. Method of measurement: Standardized questionnaire, the patients feel better, better expressed by the patient and his companions.
- Secondary Outcome Measures
Name Time Method Drug side effects. Timepoint: Just after the intervention until a week later. Method of measurement: Questionaire, Physical exam.;Worsening of the patient. Timepoint: Just after the intervention until a week later. Method of measurement: Questionaire, Physical exam.;Treatment failure. Timepoint: Just after the intervention to one hour after the start of intervention. Method of measurement: Physical examination.