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NCT05232955
Investigations of the Pathophysiology of Gilles de la Tourette Syndrome. Part 1: Simultaneous PET and 3T MRI
trial testing PET/MR scanner in Gilles de la Tourette Syndrome in 40 participants. Completed in 4 July 2023.
6 April 2023
Quick facts
| Lead sponsor | Max Planck Institute for Human Cognitive and Brain Sciences |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 40 |
| Start date | 4 May 2022 |
| Primary completion | 6 April 2023 |
| Estimated completion | 4 July 2023 |
| Sites | 1 location across Germany |
Drugs / interventions tested
- PET/MR scanner
Conditions studied
- Gilles de la Tourette Syndrome — all drugs for Gilles de la Tourette Syndrome →
- Tourette Syndrome — all drugs for Tourette Syndrome →
Sponsor
Max Planck Institute for Human Cognitive and Brain Sciences
Who can join
Adults 18 to 50, any sex, with Gilles de la Tourette Syndrome or Tourette Syndrome. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Gilles de la Tourette syndrome (GTS; also known as Tourette syndrome) is a congenital neuropsychiatric disorder. Characteristic symptoms are so-called tics-rapid, repetitive movements (motor tics) or vocalizations (vocal tics) that start suddenly without any apparent purpose. Previous research supports the hypothesis of defective regulation (dysregulation) of the dopaminergic system, with particular discussion of dysfunction of tonic/phasic dopamine release or dopaminergic hyperinnervation. Moreover, given the complex interaction of different neurotransmitters, especially in the basal ganglia, it can be assumed that abnormal dopaminergic transmission also affects other transmitter systems, such as glutamate (Glu) or γ-aminobutyrate (GABA). Furthermore, recent results suggest an abnormality in cerebral iron metabolism in GTS. Since iron is accumulated in dopamine vesicles and plays a central role in dopamine synthesis, this observation may also be related to dysfunction of the dopaminergic system. Therefore, in this multimodal study, the investigators aim to combine positron emission tomography (PET), magnetic resonance imaging (MRI), and magnetic resonance spectroscopy (MRS) methods comparing patients with GTS and a control cohort. In Part 1 of this study, MRI and MRS at 3 Tesla are employed to investigate (i) the binding potential of D1 dopamine receptors, (ii) the concentrations of Glu, glutamine and GABA in the corpus striatum and the cortex cingularis anterior and (iii) the subcortical iron concentration.
Publications & conference data
2 peer-reviewed publications reference this trial (live from Europe PMC):
-
Abnormalities of iron homeostasis and the dopaminergic system in Tourette syndrome revealed by 7T MRI and PET.
Gkotsoulias DG, Rullmann M, Schmitt S, Bujanow A, et al · · 2025 · cited 3× · PMID 40177529 · DOI 10.1093/braincomms/fcaf104 -
CRISPR/Cas9 in colorectal cancer: Revolutionizing precision oncology through genome editing and targeted therapeutics.
Alhasso B, Shareef A, Baldaniya L, Oweis R, et al · · 2025 · PMID 40896696 · DOI 10.22038/ijbms.2025.87531.18902
Verify or expand the search:
- PubMed search for NCT05232955
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Currently open trials in the same condition.
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05232955 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Max Planck Institute for Human Cognitive and Brain Sciences
- Last refreshed: 1 April 2024
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05232955.
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