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Evaluation of the effect of nano-based inhalation solution to relieve shortness of breath in COVID-19 patients

Evaluation of the effect of inhaled solution based on silver colloid with the brand name colloide silver nasal spray 10ppm to control COVID-19-induced lung infection and increase patients' respiratory volume

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190226042851N1
Enrollment
40
Registered
2020-10-05
Start date
2020-08-22
Completion date
Unknown
Last updated
2020-10-06

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

Conditions

sars-covid-19 - covid-19. COVID-19 Disease

Interventions

Intervention 1: Intervention group: In addition to receiving the drug according to the national protocol, this group uses the drug under study by inhalation. The national protocol uses interferon beta

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Positive PCR test The patient is not COPD Not having acute kidney problems The patient does not have Acute liver failure 18 years and older The patient does not need ventilator therapy The patient has low respiratory capacity The patient has covide-19

Exclusion criteria

Exclusion criteria: The patient is hospitalized for less than seven days

Design outcomes

Primary

MeasureTime frame
The patient's respiratory capacity. Timepoint: Before reading And is monitored daily during the study. Method of measurement: Encouraging spirometry device - pulse oximeter - clinical examination.;Control of the patient's pulmonary infection. Timepoint: Clinical examinations and measurements of the patient's body temperature are performed daily before the study and during the study - the patient's CT scan is taken before the start of the study and at the end of the study. Method of measurement: Clinical examinations - mercury thermometer - CT scan.

Secondary

MeasureTime frame
Compelet blood count. Timepoint: The first and last day of the study are monitored. Method of measurement: Blood sampling from the patient.;Alkaline Phosphatase. Timepoint: The first and last day of the study are monitored. Method of measurement: Blood sampling from the patient.;Urine analysis. Timepoint: The first and last day of the study are monitored. Method of measurement: Urine sampling of the patient.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHakim abiavy

Ahvaz University of Medical Sciences

hakim.abiavy76@gmail.com0613787287

Outcome results

None listed

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