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Effects of Intravenous (IV) Citalopram on Emotional Brain Activity in Healthy Young and Elderly Adults

R

Rotman Research Institute at Baycrest

Status

Terminated

Conditions

Healthy Young and Elderly Volunteers

Treatments

Drug: Normal Saline
Drug: Intravenous Citalopram

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Antidepressant medications known as selective serotonin reuptake inhibitors (SSRIs) are most commonly prescribed to treat depression and anxiety. How antidepressants work on the brain to alter mood and behaviour is not well understood. This study will use a brain scanning technique (functional magnetic resonance imaging) to examine how aging impacts brain activation during emotional tasks after the administration of intravenous (IV) citalopram (this is the only SSRI available in this form, and is well tolerated and safe in young and old adults). The investigators will further determine what role genetic differences play in this relationship. The investigators expect to see an increase in brain signal as the concentration of IV citalopram increases. However, the investigators propose that the brain signal in older adults will not be as strong as in younger adults. Furthermore, the investigators expect that participants genetically predisposed to have fewer serotonin transporters (the site of action of SSRIs) will show greater decreases in brain activation with citalopram.

Enrollment

29 patients

Sex

Male

Ages

20+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Male aged 60 or older (elderly group)
  • Male aged 20-40 (younger adult group)
  • English speaking
  • Right-handed
  • Non-smoker
  • Score of 27 or greater on the Mini Mental State Exam

Exclusion criteria

  • Unstable medical, cardiac, or neurological illness (including stroke, brain tumour, epilepsy, significant head injury, Alzheimer's, Parkinson's or Huntington's disease)
  • Laboratory results indicating unanticipated illness or intolerability of blood drawing procedures or of study drug
  • Current or lifetime Axis-I psychiatric diagnosis on the DSM-IV/SCID (i.e., Module A: Mood, Module F: Anxiety, Module B & C: Psychosis)
  • History of drug or alcohol abuse within one year, or lifetime history of alcohol or drug dependence (i.e., SCID Module E: Substance Abuse, or clinically significant urine toxicology screen)
  • History of non-tolerance to SSRI therapy; including history of SSRI-related syndrome of inappropriate antidiuretic hormone secretion (SIADH) or sinus bradycardia on ECG (less than 50 beats per minute)
  • Contraindication to MRI (as per MRI Contraindication Screening Form)

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Quadruple Blind

29 participants in 2 patient groups, including a placebo group

Intravenous Citalopram
Experimental group
Treatment:
Drug: Intravenous Citalopram
Normal Saline
Placebo Comparator group
Description:
250mL of 0.9% Sodium Chloride Solution
Treatment:
Drug: Normal Saline

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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