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Efficacy of Nebulized Lidocaine, Salbutamol, and Beclomethasone Plus Salbutamol in the Covid-19 Patients With ARDS on Non-invasive Ventilation; Randomized Control Trial

Efficacy of Nebulized Lidocaine, Salbutamol, and Beclomethasone Plus Salbutamol in the Covid-19 Patients With ARDS on Non-invasive Ventilation; Randomized Control Trial

Status
UNKNOWN
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04979923
Enrollment
81
Registered
2021-07-28
Start date
2021-07-01
Completion date
2021-08-31
Last updated
2021-07-28

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

Conditions

COVID-19 Acute Respiratory Distress Syndrome

Brief summary

The COVID-19, a pandemic as declare by WHO1, has a devastating impact on health and economic worldwide2. Literature suggests that acute respiratory distress syndrome (ARDS) develops over 20% of the infected individuals with Coivd-pneumonia3 along with other symptoms like fever followed by cough and dyspnea as well as chest pain in severe cases4. The current preventative strategies are non-specific10, and current interventions are predominantly supportive1. Recently, some studies have demonstrated anti-inflammatory actions for local anesthetics including lidocaine.

Interventions

DRUGLidocaine

Lidocaine will be used for nebulization of the covid-19 patients and will be compared with other two drugs

Sponsors

Sheikh Zayed Medical College
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Covid-19 positive * Moderate to severe ARDS

Exclusion criteria

* patients with COPD or taking bronchodilators and steroids for chronic respiratory illnesses

Design outcomes

Primary

MeasureTime frameDescription
Cough suppressionwithin five minutes of initiation of treatment it will be assessedit will be assessed by using cough severity score

Secondary

MeasureTime frameDescription
correction of hypoxiaimmediately before and after interventionit will be assessed by PaO2

Countries

Pakistan

Contacts

Primary Contactsairah s sadaf, FCPS
sairahbabar@live.com0092 689230165

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026