Combined superficial and deep cervical plexus block versus patient-controlled analgesia (PCA) in patients undergoing total laryngectomy

Combined superficial and deep cervical plexus block versus patient-controlled analgesia (PCA) in patients undergoing total laryngectomy; a comparative study

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

PACTR

Registry ID

PACTR202403682323400

Enrollment

Registered

2024-03-28

Start date

2024-03-01

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

Cancer Ear, Nose and Throat Surgery Anaesthesia

Interventions

Group1 CPB Cervical Plexus Block

Group2 PCA Patient Controlled Analgesia

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Adult patients of both genders, aged between 18 and 65 years. 2. American society of Anesthesiologists (ASA) physical status I and II. 3. Patients undergoing total laryngectomy.

Exclusion criteria

Exclusion criteria: 1. Body mass index (BMI) more than 35 kg/m2. 2. Patients with neuromuscular diseases. 3. Patients with bleeding or coagulation disorders. 4. Patients with psychiatric disorders. 5. Presence of infection at the site of injection. 6. Presence of allergy to any of medications used in this study.

Design outcomes

Primary

Measure	Time frame
Pain score measured by visual analogue score (VAS).	—

Secondary

Measure	Time frame
Cumulative fentanyl consumption.;Heart rate (HR) and mean arterial pressure (MAP).;Time of the first rescue analgesia.;Duration of surgery.;Length of hospital stay.;Incidence of postoperative side effects (nausea, vomiting, and pruritus).	—

Countries

Egypt

Contacts

Public ContactMohamed Nashaat Mohamed

Mohamed N. Mohamed

Moh_nashaat@mans.edu.eg+201092323198

Outcome results

None listed

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