ISRCTN81508784CompletedNot Applicable
Botulinum toxin in the treatment of orofacial tardive dyskinesias: a single blind study
Parnassia Psycho-medical Centre (Netherlands)0 sites14 target enrollmentStarted: March 8, 2006Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Enrollment
- 14
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Sex
- All
Inclusion Criteria
- •1. Patients suffering from orofacial tardive dyskinesias for at least 3 months
- •2. Stable dosage of psychopharmacological medication
- •3. Written informed consent by the patient
Exclusion Criteria
- •1. Age younger than 18 years
- •2. Contraindication for botulinum toxin (myasthenia gravis, Lambert Eaton Myasthenic Syndrome)
- •3. Women known to be pregnant or having a positive pregnancy test
Investigators
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