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The role of the serotonin transporter in citalopram pharmacological MRI

The role of the serotonin transporter in citalopram pharmacological MRI - SERT-phMRI

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON42073
Enrollment
45
Registered
2014-10-27
Start date
2014-12-05
Completion date
Unknown
Last updated
2024-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

serotonine systeem NA

Interventions

None listed

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Three groups of N = 15 each: healthy female volunteers, aged between 18 and 30 without any harddrug exposure including MDMA.

Exclusion criteria

Exclusion criteria: Serious general medical condition or one that could interfere in the interpretation of results, use of (5-HT) medication or supplements and / or illicit (hard) drug use within the last 2 weeks, excessive consumption of alcohol (>21 units/ week), caffeine (greater than eight cups of coffee per day) or cigarette (greater than 15 cigarettes per day), allergy to iodine tablets, contraindications for MRI (e.g. ferromagnetic osteosynthetic material, pacemaker, artificial cardiac valves, claustrophobia), abnormal ECG, or pregnant (a pregnancy test will be administered every visit).

Design outcomes

Primary

MeasureTime frame
1. Change score in thalamic [123I]FP-CIT binding ratio between SPECT scan 1 and 2 (i.e. SERT occupancy), and the interaction effect with citalopram dose. 2. Change score in thalamic CBF (phMRI study). This is the difference between baseline CBF and post-citalopram CBF scores. The interaction effect of delta CBF scores and citalopram dose will also be assessed. Endpoint: association between SERT occupancy and delta CBF.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)