OLFACTION AND BIPOLAR DISODER

NCT ID: NCT06809881

Last Updated: 2025-09-02

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 240 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2016-01-01
• Study Completion Date: 2020-01-01

Brief Summary

To compare olfactory performance between patients with BD and HC and correlate their performances to neuroimaging data

Conditions

Bipolar Disorder

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: NONE

Study Groups

Controls

n= 40 Healthy subjects

Group Type: OTHER

olfactory testing, MRI acquisition, clinical assessment

Intervention Type: OTHER

Patients

n=100 Patients with bipolar disorder

Group Type: OTHER

olfactory testing, MRI acquisition, clinical assessment

Intervention Type: OTHER

Interventions

olfactory testing, MRI acquisition, clinical assessment

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Patients with BD and HC
• Fluent in french
• Having a public health insurance
• Not being on tutorship

Exclusion Criteria

• Family history of bipolar disorder for controls
• Alcohol dependence

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Institut National de la Santé Et de la Recherche Médicale, France

OTHER_GOV

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Inserm U 955 Eq 15

Créteil, VAL DE MARNE, France

Countries

France

References

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Other Identifiers

C15-06

Identifier Type: -

Identifier Source: org_study_id