Trials / Completed
CompletedNCT04793984
Efficacy and Safety Evaluation of Inhaleen Inhalation in Hospitalized COVID-19 Patients
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 14 (actual)
- Sponsor
- Marinomed Biotech AG · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The current study will investigate the tolerability and efficacy of inhaled Carragelose® versus saline in hospitalized COVID-19 patients. As SARS-CoV-2 replicates readily in the lung, it is planed to apply Carragelose® in an inhalative form. Hospitalized COVID-19 patients with respiratory symptoms will inhale Inhaleen for 5 days.
Detailed description
The tolerability and efficacy of inhaled Carragelose® will be investigated in a randomized, double blind, placebo-controlled trial in hospitalized COVID-19 patients. Patients will inhale Inhaleen or Placebo 3 times a day for 7 minutes for 5 days. The primary objective of the trial is to demonstrate that Inhaleen inhalation improves the clinical status of hospitalized COVID-19 patients on day 8 compared to placebo inhalation.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Carragelose | inhalation 3 times a day |
| DEVICE | NaCl | inhalation 3 times a day |
Timeline
- Start date
- 2021-03-08
- Primary completion
- 2022-07-30
- Completion
- 2022-07-30
- First posted
- 2021-03-11
- Last updated
- 2022-08-29
Locations
1 site across 1 country: Austria
Source: ClinicalTrials.gov record NCT04793984. Inclusion in this directory is not an endorsement.