Skip to content

A study comparing two methods of numbing the nose (spray device vs cotton pledgets) to make nasal endoscopy more comfortable.

Comparative evaluation of intranasal mucosal atomization device (MAD) with nasal pledgets to topicalize nasal passages for nasal endoscopy. - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/09/094805
Enrollment
42
Registered
2025-09-15
Start date
Unknown
Completion date
Unknown
Last updated
2025-10-13

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

Conditions

Health Condition 1: C00-C14- Malignant neoplasms of lip, oral cavity and pharynx

Interventions

Intervention1: Intranasal mucosal atomization device (MAD) to topicalize nasal passages for nasal endoscopy: Comparative evaluation of intranasal mucosal atomization device (MAD) with nasal pledgets t

Sponsors

Department of Anaesthesiology,Kasturba Medical College,MAHE
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients scheduled for elective nasal endoscopy for elective surgeries will be considered for inclusion. 2.Adult patients aged 18 years and above will be included in the study. 3.Both male and female adult patients will be included in the study. 4.Patients with ASA physical status I-II will be considered for inclusion.

Exclusion criteria

Exclusion criteria: 1)Patients with a history of or having current tumor pathologies involving the nasal cavity will be excluded from the study 2)Patients with bleeding disorders or a history of coagulation disorders will be excluded from the study. 3)Pregnant individuals will be excluded from the study. 4)Individuals with a history of psychiatric disorders affecting cooperation or communication during the procedures will be excluded. 5)Individuals with a history of chronic use of nasal medications that may interfere with the study outcomes will be excluded. 6)Patients with any acute nasal infections or inflammation on the day of the scheduled procedure will be excluded

Design outcomes

Secondary

MeasureTime frame
NILTimepoint: NIL

Primary

MeasureTime frame
To compare the patient comfort during passage of nasal endoscope following topicalization of nasal passage with intranasal mucosal atomization device (MAD) or nasal pledgets.Timepoint: Numeric pain rating score will be asked after insertion of nasal endoscope, after 15 minutes of topicalization.

Countries

India

Contacts

Public ContactDIKSHA MELBA DMELLO

Kasturba Medical College,MAHE

savankum@gmail.com8105308865

Outcome results

None listed

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