Ireland
--:--IST
Latest
Astellas Expands Its 330 Million Euro Tralee Biopharma Facility with a Second Aseptic Filling Line to Double Drug-Product Capacity Xeolas Pharmaceuticals Opens 158,000 Sq Ft State-of-the-Art Baldoyle Facility to Scale Specialty Medicine Manufacturing Priya Life Science Partners with Fleming for the 9th Annual Corporate Compliance & Transparency in Life Sciences Summit in Zurich Ireland Has the Capital and the Lessons: Digital Project Management Is How They Become Delivery Dunbar Pharma Brings First Plant-Derived Dronabinol API to UK Market Through IPS Pharma Leveraging Priya Life Science as a Data Tracker: The Ultimate Use Case & Career Guide The €100K Reality Check: Why a Six-Figure Pharma Salary in Ireland Feels Different Than in Switzerland or Germany Ireland's €93.8 Billion Non-EU Pharma Export Engine: 2025 Eurostat Trade Data and Economic Impact Astellas Expands Its 330 Million Euro Tralee Biopharma Facility with a Second Aseptic Filling Line to Double Drug-Product Capacity Xeolas Pharmaceuticals Opens 158,000 Sq Ft State-of-the-Art Baldoyle Facility to Scale Specialty Medicine Manufacturing Priya Life Science Partners with Fleming for the 9th Annual Corporate Compliance & Transparency in Life Sciences Summit in Zurich Ireland Has the Capital and the Lessons: Digital Project Management Is How They Become Delivery Dunbar Pharma Brings First Plant-Derived Dronabinol API to UK Market Through IPS Pharma Leveraging Priya Life Science as a Data Tracker: The Ultimate Use Case & Career Guide The €100K Reality Check: Why a Six-Figure Pharma Salary in Ireland Feels Different Than in Switzerland or Germany Ireland's €93.8 Billion Non-EU Pharma Export Engine: 2025 Eurostat Trade Data and Economic Impact
Starting soon Not applicable

Let It TiC in Childhood Provisional Eye Tic

NCT07838428 · tracked via the Priya Life Science China tracker
Phase
Not applicable
Started
2026-10-01
Last updated
2026-09-24

Condition(s) studied

Tic DisorderProvisional Tic Disorder

Investigational drug(s) / intervention(s)

Reducing Attentional Interventions Therapy TreatmentContinue with the previous treatment plan

Reducing Attentional Interventions Therapy Treatment: Reducing Attentional Interventions Therapy Treatment

Continue with the previous treatment plan: Continue with the previous treatment plan

Study summary

Clarify the effectiveness and safety of "Reduced-Attention Intervention Therapy" in treating children with Provisional tic disorder (PTD) who mainly exhibit abnormal blinking behavior

Eligibility

Sex
ALL
Min age
6 Years
Max age
14 Years
Healthy volunteers
No
Inclusion Criteria: 1. Age: Between 6 and 14 years old 2. the diagnosis is PTD characterized by abnormal blinking as the main manifestation 3. The legal guardian agrees and signs the informed consent form, and complies with the research protocol Exclusion Criteria: 1. Received any other behavioral intervention treatment or took related therapeutic drugs within the past 3 months. 2. The current active allergic diseases 3. There are any eye disorders that may cause confusion in the interpretation of the research results 4. Having worn contact lenses within the past 3 months 5. The researchers determined that the participants were not suitable to participate in this study due to other reasons

Primary outcome measure(s)

  • Score of the Yale Comprehensive Tics Severity Scale — through study completion, an average of 6 months
    Three evaluation researchers who had undergone unified training and were unaware of the group assignments independently conducted blinded scoring based on the standardized protocol and the medical records provided by the same guardian of the patients. The average value was then calculated.

Trial sites (1)

FacilityCityRegionStatus
Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, Guangdong 510080 Guangzhou China
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07838428 on ClinicalTrials.gov ↗ ← All trials in China