Iloprost

A prostacyclin analogue.

Phase of research

Potential treatment - theoretical effect

How it helps

Antiviral

Drug status

Used to treat other disease

1
Supporting references
0
Contradictory references
4
AI-suggested references
2
Clinical trials

General information

Iloprost on PubChem


Marketed as

VENTAVIS

 

Structure image - Iloprost

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Supporting references

AI-suggested references

Clinical trials

ID Title Status Phase Start date Completion date
NCT04420741 Infusion of Prostacyclin (Iloprost) vs Placebo for 72-hours in COVID-19 Patients With Respiratory Failure Completed Phase 2 Jun/15/2020 Apr/23/2021
  • Alternative id - COMBAT-COVID-19|2020-001296-33
  • Interventions - Drug: Iloprost|Drug: Isotonic saline
  • Study type - Interventional
  • Study results - No Results Available
  • Locations - Dept. of Anaesthesia and Intensive Care, Bispebjerg Hospital, Copenhagen, Denmark|Dept. of Intensive Care, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark|Dept. of Intensive Care, Copenhagen University Hospital Herlev, Herlev, Denmark|Dept. of Anaesthesia and Intensive Care, Nordsjaelands Hospital, Hillerød, Denmark|Dept. of Anaesthesia and Intensive Care, Hvidovre Hospital, Hvidovre, Denmark
  • Study designs - Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)|Primary Purpose: Treatment
  • Enrollment - 80
  • Age - 18 Years and older   (Adult, Older Adult)
  • Outcome measures - Mechanical ventilation free days|28 and 90-day mortality|Modified Sequential Organ Failure Assessment (SOFA)|Vasopressor free days|Renal replacement free days|Serious adverse reactions (SARs)|Serious adverse events (SAEs)
NCT04445246 Inhaled Iloprost for Suspected COVID-19 Respiratory Failure Recruiting Phase 2 May/23/2020 May/31/2021
  • Alternative id - MRC-05-026
  • Interventions - Drug: Inhaled ILOPROST
  • Study type - Interventional
  • Study results - No Results Available
  • Locations - Hamad Medical Corporation, Doha, Qatar
  • Study designs - Allocation: N/A|Intervention Model: Single Group Assignment|Masking: None (Open Label)|Primary Purpose: Treatment
  • Enrollment - 40
  • Age - 18 Years and older   (Adult, Older Adult)
  • Outcome measures - change in oxygenation parameters|Rates of endotracheal intubation|Invasive ventilation duration|ICU length of stay|Hospital Length of stay|Rates of proning therapy|Rates of ECMO cannulation|Mortality