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A clinical trial of NanoAgCide hand sanitizer on Coronavirus patients.

A prospective open label clinical trial to evaluate the topical viral load reduction potential of Colloidal Silver (NanoAgCideTM) based hand sanitizer on SARS-CoV-2 infected subjects.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/10/028688
Enrollment
20
Registered
2020-10-28
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Interventions

Intervention1: Colloidal Silver (NanoAgCideTM): Active Ingredient: Colloidal Silver (B.P.) 50 ppm 12 sprays on each hand -wait for 60 sec, rub hands for 30 seconds, Control Intervention1: NA: NA

Sponsors

WeInnovate Biosolutions Pvt Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Male or Female aged 18 to 80 years (both inclusive) of age tested SARS-CoV-2 positive within last 8 days of study enrolment. 2. Patients willing to sign written informed consent and are ready to comply to study procedure. 3. SARS-CoV-2 positive asymptomatic or symptomatic patients who are under institutional quarantine.

Exclusion criteria

Exclusion criteria: 1. Patients requiring emergency treatment during enrolment. 2. Patients on ventilator support. 3. Pregnant or lactating woman. 4. Subjects with history of sun burn on hands. 5. Subjects with history of skin disorders or on medication for the same: Eczema, Urticaria, Psoriasis, Herpes, skin cancer, Lupus, Vitiligo, Fungal infection, Candidiasis. 6. Subjects on treatment of any degree burns. 7. Any kind of psychiatric disorder or a condition in the opinion of the investigator may hinder communication with the research team. 8. Inability of the subject to cooperate or communicate with the research team.

Design outcomes

Primary

MeasureTime frame
Clinically significant Quantitative Reduction of 80% Virus load from baseline to EOT. Timepoint: 90 secs

Secondary

MeasureTime frame
Time taken by the IP in Quantitative Reduction of Virus from baseline to EOT in a given period of time.Timepoint: 90 secs

Countries

India

Contacts

Public ContactSubham Dutta

WeInnovate Biosolutions Pvt. Ltd

wibcto@gmail.com9890999625

Outcome results

None listed

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