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Optimizing Tracheostomy Anesthesia: A Comparative Study of Nerve Blocks

Optimizing Tracheostomy Anesthesia: A Comparative Study of Nerve Blocks

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
PACTR
Registry ID
PACTR202407555927073
Enrollment
120
Registered
2024-07-18
Start date
2024-06-01
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Ear, Nose and Throat Anaesthesia

Interventions

Bilateral Superficial Cervical Plexus Block with Bilateral Superior Laryngeal Nerve Block

Sponsors

Faculty of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Eligible patients must fall within the age range of 18 to 75 years have a clinical requirement for tracheostomy, be classified as American Society of Anesthesiologists (ASA) categories I to III possess the capability to give informed consent.

Exclusion criteria

Exclusion criteria: contraindications to regional anesthesia a history of allergies to local anesthetics pregnancy inability to provide informed consent.

Design outcomes

Primary

MeasureTime frame
incidence of coughing and laryngospasm during the tracheostomy procedure.

Secondary

MeasureTime frame
postoperative pain scores, complications, and patient satisfaction.

Countries

Egypt

Contacts

Public ContactAsmaa Abd Elhameed

Lecturer Medical Statistics Medical Research Institute Alexandria university

asmaa.hassan@alexu.edu.eg+201001831803

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026