TESTING OF HAND SANITIZER.

An open label, prospective, randomized parallel group study to evaluate the comparative efficacy of sterlomax hand sanitizer with marketed products

Status

Active, not recruiting

Phases

Phase 1Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2021/08/035597

Enrollment

300

Registered

2021-08-11

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

None listed

Interventions

Intervention1: STERLOMAX HAND SANITIZER: Single dose (3 ml) for topical use. Applied once only in complete study. Control Intervention1: MARKETED HAND SANITIZERS: Single dose (3 ml) for topical use. A

Eligibility

Inclusion criteria

Inclusion criteria: a. Volunteer/ Healthcare providers working in high risk area of hospital like OTs, ICUs, HDUs etc. b. Volunteer aged between 18-60 years (both inclusive) c. No bruises on the palms and proven to be healthy d. Willing to give written consent to participate e. Preference for hospital staff and no infected patients which visiting hospital.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
a) Significance decrease in the bioburden/ microbial load. b) Elimination of pathogenic organisms from body surfaces of working health care providers in high risk area of hospital. c) Minimal time taken by hand sanitizer to show microbial inhibition. d) Maximum time hand sanitizer can sustain its anti-microbial action. Timepoint: Two time points for individual. One before applying the sanitizer and one after applying the sanitizer.	—

Measure

Time frame

a) Significance decrease in the bioburden/ microbial load. b) Elimination of pathogenic organisms from body surfaces of working health care providers in high risk area of hospital. c) Minimal time taken by hand sanitizer to show microbial inhibition. d) Maximum time hand sanitizer can sustain its anti-microbial action. Timepoint: Two time points for individual. One before applying the sanitizer and one after applying the sanitizer.

—

Secondary

Measure	Time frame
a) Significance decrease in the bioburden/ microbial load. b) Elimination of pathogenic organisms from body surfaces of working health care providers in high risk area of hospital. c) Minimal time taken by hand sanitizer to show microbial inhibition. d) Maximum time hand sanitizer can sustain its anti-microbial action. Timepoint: 1 Year	—

Countries

India

Contacts

Public ContactNavid Reza Shahtaghi

Guru Nanak Dev University, Amritsar

navid_255@yahoo.com9620324643

Outcome results