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THE EFFICACY OF PVP-I GARGLES AND INTRANASAL INSTILLATION ON CHECKING THE PROGRESSION OF COVID 19

TO ASSESS THE EFFICACY OF POVIDONE IODINE GARGLES AND INTRANASAL INSTILLATION ON CHECKING THE PROGRESSION OF THE COVID-19 DISEASE AND VIRAL LOAD - A PROSPECTIVE RANDOMISED AND CONTROLLED STUDY

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/10/037563
Enrollment
100
Registered
2021-10-26
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: B972- Coronavirus as the cause of diseases classified elsewhere Health Condition 2: J988- Other specified respiratory disorders

Interventions

Intervention1: Betadine gargle and Nasal drops: Patients meeting inclusion and exclusion criteria will be identified and an informed, written consent will be obtained. The patients will randomly be al

Sponsors

DR S P AMBESH
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: COVID 19 positive by RT PCR analysis of nasopharyngeal/oropharyngeal specimens Patients admitted with mild COVID 19 infection with or without co morbidities.

Exclusion criteria

Exclusion criteria: Patients with tachypnoea Patients with SpO2less than 94% on room air Patients requiring oxygen supplementation or assisted ventilation at admission. Patients receiving antiviral agents Patients with known sensitivity to PVP-I. Pregnant patients and patients with thyroid diseases. Patients who refuse or are incapable of giving consent

Design outcomes

Primary

MeasureTime frame
1)To evaluate the efficacy of intranasal povidone iodine 1% solution and gargles in reducing the viral load of SARS CoV2 in nasopharynx of patients admitted with mild COVID 19 disease. 2)To evaluate clinical course in patients with mild COVID 19 illness who were treated with PVP-I gargle and intranasal solution with respect to ,Progression of disease Radiological features Inflammatory markers Timepoint: At baseline,at 1 week

Secondary

MeasureTime frame
1)To assess tolerability of PVP-I as gargle and intranasal solution in COVID 19 patients. 2)To study if intranasal Povidone Iodine 1% and gargles administration can reduce the duration of hospital stay among patients admitted with mild COVID 19 disease. Timepoint: 1 week

Countries

India

Contacts

Public ContactDR ANUSREE EV

SGPGIMS,LUCKNOW

anusree442@gmail.com9446624218

Outcome results

None listed

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