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Adult Tic Disorders Registry (RegisTICs)

A

Assistance Publique - Hôpitaux de Paris

Status

Enrolling

Conditions

Tic Disorders

Treatments

Other: QOL to be completed by the participant

Study type

Observational

Funder types

Other

Identifiers

NCT05090943
APHP210801

Details and patient eligibility

About

The purpose of this study is to develop the adult tic disorders registry in order to characterize the relationship between tic severity and tic-related impairment in women compared to men with tic disorders.

Enrollment

450 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria :

  1. Age >18 years
  2. Patients with Tic disorders
  3. Given the non-opposition

Non Inclusion criteria

  1. No affiliation to a French health social insurance
  2. Significant congenital disorders that may affect understanding of assessments
  3. Patients under guardianship or curatorship

Trial design

450 participants in 1 patient group

Quality of life questionnaires
Treatment:
Other: QOL to be completed by the participant

Trial contacts and locations

7

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Central trial contact

Emmanuel Flamand-Roze, MD, PhD

Data sourced from clinicaltrials.gov

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