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Comparing Atomizer device with Cotton-Tipped Swabs for Transnasal Ganglion Block in Head and Neck Cancer patients for pain relief.

To evaluate the clinical performance of Laryngo-Tracheal Mucosal Atomizer versus cotton tipped swabs for administering transnasal pterygopalatine ganglion block in head and neck cancer patients: a randomized clinical trial. - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/084608
Enrollment
140
Registered
2025-04-11
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Health Condition 1: C060- Malignant neoplasm of cheek mucosa

Interventions

Intervention1: Atomizer: use of Laryngo-Tracheal Mucosal Atomizer device in nasal cavity for chronic pain relief in head and neck cancer patients. Control Intervention1: cotton swab: use of traditiona

Sponsors

Kalyan Singh Superspeciality cancer institute
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients of head and neck cancer with moderate to severe pain. 2.Patient on oral morphine whose pain is not well controlled.

Exclusion criteria

Exclusion criteria: 1.Patients with nasal obstruction, nasal septal deviation, polyp, nasopharyngeal growth. 2.history of nasal bleeding, bleeding diathesis 3.Intracranial extension of disease, 4.Recent nasal, or sinus surgery. 5.patient refusal to participate 6.Patients who are allergic to local anaesthetics.

Design outcomes

Primary

MeasureTime frame
Pain score (VAS) before intervention, after 15 minutes of administering block and then followed at 1 hour, 8 hours and 24 hoursTimepoint: Pain score (VAS) before intervention, after 15 minutes of administering block and then followed at 1 hour, 8 hours and 24 hours

Secondary

MeasureTime frame
1. Patient satisfaction score 2. Rescue dose of Morphine taken by patient 24 hrs before and for breakthrough pain during 24 hours. 3. Any other side effects associated with block like epistaxis etc Timepoint: 1. at 24 hrs of block

Countries

India

Contacts

Public ContactRuchi Saxena

Kalyan Singh Superspeciality Cancer Institute

taru_ruchi@yahoo.co.in09140366422

Outcome results

None listed

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