Clinical Trials Directory

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UnknownNCT05840861

Using 18F-FPEB PET to Identify mGLUR5 Availability in Affective Disorders

Status
Unknown
Phase
Study type
Observational
Enrollment
59 (estimated)
Sponsor
Central South University · Academic / Other
Sex
All
Age
18 Years – 35 Years
Healthy volunteers
Accepted

Summary

Evidence suggests that mGLUR5 availability may play a key role in the biology of mood disorders. This study aimed to investigate the changes in metabotropic glutamate receptor 5 (mGLUR5) availability and clinical symptoms in patients with MDD and bipolar disorder(BD) after two months of vortioxetine treatment. The investigators hypothesized that patients with MDD and BP have abnormal mGluR5 availability in certain brain regions, and baseline mGLUR5 availability can predict prognosis the prognosis of MDD and BD. fMRI and NODDI are also used to evaluate the function or neurite condition at baseline and 8 week

Conditions

Interventions

TypeNameDescription
DRUGVortioxetineAll MDD patients will receive 5mg of Vortioxetine per day at the start of this study, which will be gradually increased to 10mg per day within one week.
DRUGQuetiapineAll patients with bipolar disorder will receive 50mg of Quetiapine at day 1, 100mg of Quetiapine at day 2, 200mg of Quetiapine at day 3, and 400mg of Quetiapine per day since day 4.

Timeline

Start date
2020-11-05
Primary completion
2023-08-21
Completion
2023-09-05
First posted
2023-05-03
Last updated
2023-08-14

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05840861. Inclusion in this directory is not an endorsement.