AshLi Aerosol eliminator device - Comparing the advantages of a modified version to the previous one.

Comparison OF Original And Modified “ASHLI’ S Aerosol Eliminator - In COVID Operation Theatre " - AshLI

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/05/067415

Enrollment

Registered

2024-05-15

Start date

Unknown

Completion date

Unknown

Last updated

2024-05-27

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

Conditions

Health Condition 1: J22- Unspecified acute lower respiratory infection

Interventions

Intervention1: Original AshLis aerosol eliminator and Modified AshLis aerosol eliminator: Original AshLi s aerosol eliminator device was designed and being used in COVID operation theatre during the

Eligibility

Inclusion criteria

Inclusion criteria: 1.All the adult patients undergoing emergency and elective surgery under regional anaesthesia, at COVID operation theatre, where Ash Li aerosol eliminator is used 2.Patients who give consent to be part of the study

Exclusion criteria

Exclusion criteria: 1.Patients undergoing surgery under General anesthesia 2.Patients with altered mentation 3.Patient who cannot cooperate with the study 4.Surgeries of more than 3 hours duration

Design outcomes

Primary

Measure	Time frame
1. Reduced environmental contamination 2. Better patient and physician acceptanceTimepoint: intraoperative period and immediate postoperative( within 1 hour after surgery)	—

Secondary

Measure	Time frame
To compare the physician’s & patient’s acceptability among the two devices.Timepoint: 1	—

Countries

India

Contacts

Public ContactAsish K

Govt Medical College

asishkarthik@gmail.com9645085073

Outcome results

None listed

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