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The efficacy and safety of Choudongning capsule in Children with Tourette syndrome (TCM differentiation of phlegm stasis due to spleen deficiency ):a randomized, paralleled control, multi-center trials

The efficacy and safety of Choudongning capsule in Children with Tourette syndrome (TCM differentiation of phlegm stasis due to spleen deficiency ):a randomized, paralleled control, multi-center trials

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-13003552
Enrollment
Unknown
Registered
2013-06-20
Start date
2009-09-10
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tourette syndrome

Interventions

Test group:Choudongning capsule
positive control group:Tiapride Hydrochloride Tablets

Sponsors

First Teaching Hospital of Tianjin University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
4 Years to 18 Years

Inclusion criteria

Inclusion criteria: 1. Diagnosed as Tourette syndrome (TCM differentiation of phlegm stasis due to spleen deficiency ); 2. Aged between 4 and 18 years old; 3. Written ICF obtained from a legally acceptable representative & informed assent at Baseline as applicable by trial center's IRB/IEC.

Exclusion criteria

Exclusion criteria: 1. Involuntary movement caused by other diseases, such as rheumatism chorea, Huntington's disease, hepatolenticular degeneration, athetosis, myoclonus, acute movement disorder, hysteria seizures, epilepsy and childhood schizophrenia, drug-induced extrapyramidal symptoms and other extrapyramidal disease; 2. Transient tic disorder or Tourette associated with ADHD; 3. Epileptiform discharges were found through EEG; 4. Combined with cardiovascular, kidney and hematopoietic system or any primary disease; 5. Allergic constitution ( for two or more substances allergies ) or the preparation of known composition allergies; 6. Inability to swallow capsule or tolerate oral medication or those who are participating in other trials; 7. Those who are inclined to lose follow-up based on the investigators judgment.

Design outcomes

Primary

MeasureTime frame
Yale Global Tic Severity Scale;

Secondary

MeasureTime frame
TCM syndrome scale;

Countries

China

Contacts

Public ContactRong Ma

Tianjin University of Traditional Chinese Medicine

husiyuan1963@sina.com+86 13752009293

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026