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Tardive Dyskinesia clinical trials

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NCT ID: NCT01267188 Completed - Tardive Dyskinesia Clinical Trials

Efficacy and Safety of NBI-98854 in Subjects With Tardive Dyskinesia

Start date: January 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess the safety and efficacy of three doses (12.5, 25, and 50 mg) of NBI-98854 for the treatment of the symptoms of tardive dyskinesia (TD) in subjects with schizophrenia or schizoaffective disorder.

NCT ID: NCT00926965 Completed - Tardive Dyskinesia Clinical Trials

Tardive Dyskinesia and Cognitive Function

TD
Start date: January 2003
Phase: Phase 4
Study type: Interventional

Previous researchers indicate that impaired cognitive flexibility was the primary factor distinguishing patients with from those without tardive dyskinesia (TD)1, and cognitive dysfunction correlates positively with the severity of TD2. Longitudinal data raised the possibility that the association between cognitive dysfunction and TD may reflect not organic vulnerability to but rather a state marker for this movement disorder as "tardive dementia"3. Atypical antipsychotic had been reported to alleviate the severity of TD4 and improved neurocognitive function separately5. But no researchers ever investigated the correlation of the two effects simultaneously. This randomized, single-blind and controlled study compared the effect of atypical antipsychotic on TD, neurocognitive function and associated factors for these changes.

NCT ID: NCT00672373 Completed - Schizophrenia Clinical Trials

Extract of Ginkgo Biloba and Tardive Dyskinesia

EGBTD
Start date: December 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether Extract of Ginkgo Biloba is effective in the treatment on Tardive dyskinesia

NCT ID: NCT00401089 Completed - Obesity Clinical Trials

Efficacy Study of Panax Ginseng to Boost Antipsychotics Effects in Schizophrenia

Start date: December 2002
Phase: Phase 1/Phase 2
Study type: Interventional

The objective of the study is to determine whether Panax Ginseng with multiple interactions with key components of brain signaling pathway, can augment the effects of antipsychotics in Schizophrenia. We are primarily interested to examine the actions of Ginseng combined with antipsychotics in improving the ways patients diagnosed with schizophrenia behave in social environment, store, process and retrieve information.

NCT ID: NCT00291213 Completed - Tardive Dyskinesia Clinical Trials

Levetiracetam Treatment of Tardive Dyskinesia

Start date: n/a
Phase: Phase 3
Study type: Interventional

This is a placebo-controlled study designed to learn if levetiracetam is effective for tardive dyskinesia.

NCT ID: NCT00190008 Completed - Tardive Dyskinesia Clinical Trials

Piracetam for Treatment Tardive Dyskinesia

Start date: August 2003
Phase: Phase 3
Study type: Interventional

The mechanism involved in the development of tardive dyskinesia (TD) is complicated. It now seems that several neurotransmitter systems may be affected, including dopaminergic, noradrenergic, gamma-amino-butyric acid (GABA) ergic, cholinergic and peptidergic pathways. Piracetam (2-oxo-pyrrolidone) is a nootropic drug structurally related to GABA. It has been used clinically to treat a wide range of diseases and conditions, mainly in treatment of organic brain syndrome, myoclonus, memory impairment, post-concussional syndrome, vertigo, alcohol withdrawal, cerebrovascular insufficiency, hypoxia, intoxications of different origins or mechanic brain injures. Piracetam is cerebral homeostatic normalizer, neuroprotectant, cerebral metabolic enhancer and brain integrative agent. It enhances brain energy, especially under deficit condition: hypoxia, chemical toxicity or impaired cerebral microcirculation; preserve, protect and enhance synaptic membrane and receptor structure and plasticity. It has various effects on glutamate neurotransmission on micromolar levels piracetam potentiates potassium-induced release of glutamate from hippocampal nerves. It is an oxidant agent and may be useful for treatment TD. Piracetam is among the toxicologically safest drugs ever developed even in mega doses. Data derived from some clinical reports have suggested that piracetam can improve symptoms and is effective agent for treatment of different movement disorders including acute neuroleptic induced extrapyramidal symptoms and TD. The doses that used for TD treatment varied from 800 mg/day to 24000 mg/day. According to these findings the symptoms of TD disappeared in the period of 3-7 days. To date there was only one double-blind crossover study regarding use of piracetam for treatment TD that was conducted almost 20 years ago. The findings of this study were impressive, but to our knowledge nobody reproduced these results.

NCT ID: NCT00164242 Completed - Tardive Dyskinesia Clinical Trials

Treatment of Tardive Dyskinesia With Galantamine

Start date: January 2002
Phase: Phase 4
Study type: Interventional

Tardive dyskinesia (TD), a form of movement disorder, remains a problem for some patients who received antipsychotic medications. Increasing evidence suggests that TD may result from antipsychotic-induced dysfunction in striatal cholinergic neurons. To test whether cholinesterase inhibitors compensate for diminished cholinergic activity underlying TD, we conducted a 30-week randomized, double-blind, placebo-controlled crossover study of galantamine in 36 patients with TD.