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Finnish Dyspepsia Management -study

Finnish Dyspepsia Management -study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2008-006405-17-FI
Enrollment
Unknown
Registered
2008-11-04
Start date
2009-02-25
Completion date
Unknown
Last updated
2014-10-07

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

Conditions

Tutkimukseen rekrytoidaan n. 400 dyspepsiaoireiden vuoksi erikoissairaanhoitoon lähetettyä alle 60-vuotiasta potilasta, joiden vaiva tutkimusten jälkeen todetaan toiminnalliseksi. MedDRA version: 9.1 Level: LLT Classification code 10013946 Term: Dyspepsia

Interventions

Trade Name: Citalopram-Ratiopharm Pharmaceutical Form: INN or Proposed INN: CITALOPRAM CAS Number: 59729338 Pharmaceutical form of the placebo: Capsule* Route of administration of the placebo: Oral u

Sponsors

Kuopio University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Kts. yst. tutkimussuunnitelma kohtien E3-5 osalta Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range F.1.3 Elderly (>=65 years) F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Main Objective: Kts. yst. tutkimussuunnitelma;Secondary Objective: Kts. yst. tutkimussuunnitelma;Primary end point(s):—

Countries

Finland

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026