Serotonin Transporter Density in Late-life Depression With and Without Dementia

Melancholia Clinical Trial

Official title:

Serotonin Transporter Density in Late-life Depression With and Without Dementia

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01548937
• Other study ID #: 98-2132A
• Status: Completed
• Phase: Phase 2
• First received: December 29, 2011
• Last updated: January 27, 2016
• Start date: May 2010
• Est. completion date: December 2012

Study information

• Verified date: January 2016
• Source: Chang Gung Memorial Hospital
• Contact: n/a
• Is FDA regulated: No
• Health authority: Taiwan: Department of Health
• Study type: Interventional

Clinical Trial Summary

This study will recruit a total of 40 evaluable subjects (20 cognitively depressive, and 20 AD depressive); each evaluable subject involved in this study must fulfill all the inclusion and exclusion criteria according the subject grouping.

Safety measurement will be evaluated by medical history, vital signs, physical examinations, laboratory examinations and collecting of adverse events.

This study is expected to be completed in a period of 3 years.

Description:

Depression and dementia are the two common psychiatric disorders in the elder subjects. Alzheimer's disease (AD) is the most frequent cause of dementia and about 20% of them have depression. Depression subjects are associated with more rapid cognitive decline, a poorer response to treatment. Post mortem study showed close relationship between AD and disruptions of the serotonergic system, including loss of serotnergic neurons at brain stem. However, the alternations in presynaptic serotonin function relative to demented or non-demented subjects remain to be investigated in living subjects. In this study, the investigators will collect 40 elder subjects (i.e., age above or equal to 50 years old). The serotonin transporter activity will be compared between subjects with or without dementia using I-123 ADAM images. The single photon emission tomography (SPECT) will be compared to recent (within 6 months) F-18 FDG PET images for further investigation.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 39
• Est. completion date: December 2012
• Est. primary completion date: October 2012
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 50 Years and older

Eligibility

Inclusion Criteria:

1. Patients may be enrolled in the AD depressive group if they:

• Are males or females at least 50 years of age;

• Fulfilled the DSM-IV criteria for Major depressive disorder (APA, 1994) by MINI interview.

• Meet the NINCDS/ADRDA(National institute of Neurological and Communicative Disorders and Stroke/Alzheimer's Disease and Related Disorders Association) criteria for probable AD

• A Mini Mental State Examination (MMSE) score at screening between 10 and 24 inclusive;

• Give informed consent. If the patient is incapable of giving informed consent, the caregiver may consent on behalf of the patient (the patient must still confirm assent).

2. Patients may be enrolled in the cognitively depressive group if they:

• Are males or females at least 50 years of age;

• Fulfilled the DSM-IV criteria for Major depressive disorder (APA, 1994) by MINI interview.

• Memory function above the lower normal limits (i.e. 1.5 SD above the mean) on tests for episodic memory.

• Clinical Dementia Rating = 0. Memory Box score must be 0.

• Cognitively normal, based on an absence of significant impairment in cognitive functions or ADL.

• A MMSE score at screening > 24 for those with education level of 6 years or above and > 17 for those are illiterate;

• Give informed consent.

Exclusion Criteria:

• Pregnant or becoming pregnant during the study (as documented by pregnancy testing at screening or at any date during the study according to the PI discretion) or current breast feeding.

• Conditions affecting brain structure or function (e.g., stroke, diabetes, head trauma, depression) or use of cognitively

• Substance abuse.

• Alcohol dependence

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic

Related Conditions & MeSH terms

• Melancholia

Intervention

Drug:
• I-123 ADAM
This study will recruit a total of 40 evaluable subjects (20 cognitively depressive, and 20 AD depressive), Each evaluable subject involved in this study must fulfill all the inclusion and exclusion criteria according the subject grouping. Safety measurement will be evaluated by medical history, vital signs, physical examinations, laboratory examinations and collecting of adverse events.

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Chang Gung Memorial Hospital

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Evaluate the differences of serotonin transporter activity among depressive patient with or without dementia.	To expand the database of I-123 ADAM SPECT imaging in AD depressive and cognitively depressive patients to refine the definition of a positive scan in patient with AD and MDD.	three years	Yes
Secondary	Evaluate the relationship between the serotonin transporter activity and F-18 FDG PET image patter.	To expand the safety database of I-123 ADAM SPECT imaging Safety variables include adverse event count, lab parameters, vital signs, and ECG. Comparison will be generally made to baseline, as appropriate.	three years	Yes