F-puff_SE_2024

Status

Not yet recruiting

Phases

Phase 4

Study type

Interventional

Source

EU CTIS

Registry ID

CTIS2024-519131-42-02

Enrollment

Registered

2025-10-22

Start date

Unknown

Completion date

Unknown

Last updated

2025-12-09

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

Conditions

PAIN MANAGEMENT

Brief summary

responder rate (on NPRS scale)

Interventions

DRUGFentanyl Kalceks 50 mikrogramm/ml oldatos injekció

DRUGFentanyl Sandoz 50 mikrogramm/ml oldatos injekció

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Design outcomes

Primary

Measure	Time frame
responder rate (on NPRS scale)	—

Countries

Hungary

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026