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Pilot study on the safety and feasibility of intravenous opioid agonist therapy (OAT) with Hydagelan® (hydromorphone hydrochloride) in Vienna.

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-519652-90-01
Acronym
SHW01
Enrollment
30
Registered
2025-02-17
Start date
2025-02-17
Completion date
2025-11-30
Last updated
2025-11-10

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

Conditions

and is associated with concomitant diseases and increased mortality., encompasses various psychological and physical dimensions, Opioid dependence: Opioid dependence is a serious and usually chronic disease that requires treatment

Brief summary

- Reduction of intravenous opioid use outside the medical setting. - Feasibility of implementation and execution

Detailed description

- Reduction in co-drug use - Safety of the intervention - Improvement in health status - Retention in treatment

Interventions

DRUGHydagelan 50 mg/ml Injektions-/Infusionslösung
DRUGHydagelan 10 mg/ml Injektions-/Infusionslösung
DRUGHydagelan 20 mg/ml Injektions-/Infusionslösung

Sponsors

Suchthilfe Wien gGmbH
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
- Reduction of intravenous opioid use outside the medical setting. - Feasibility of implementation and execution

Secondary

MeasureTime frame
- Reduction in co-drug use - Safety of the intervention - Improvement in health status - Retention in treatment

Countries

Austria

Outcome results

None listed

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