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The effect of a gastric bypass procedure on the pharmacokinetics of citalopram

The effect of a gastric bypass procedure on the pharmacokinetics of citalopram - CITA study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON57704
Enrollment
6
Registered
2013-04-15
Start date
2014-04-10
Completion date
Unknown
Last updated
2025-09-08

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

Conditions

bariatrische chirurgie depression gastric bypass

Interventions

None listed

Sponsors

Maasstadziekenhuis
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: The participant is on the waiting list for gastric bypass surgery and using oral citalopram whithout changes in dosages for at last three months.

Exclusion criteria

Exclusion criteria: Persons who previously have undergone bariatric surgery.

Design outcomes

Primary

MeasureTime frame
Main study parameters / endpoints: AUC (area under the serum concentration-time curve) of citalopram.

Secondary

MeasureTime frame
Secondary study parameters / endpoints: - Outcome of depression questionnaire - Cmax (maximum serum concentration), Tmax (time of maximum serum concentration) and T1 / 2 (half-life)

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)