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Analgesic Effect of Superficial Cervical Plexus Block in Postoperative Neck Surgeries

NCT07539935 · Status: ACTIVE_NOT_RECRUITING · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2026-04-23

No results posted yet for this study

Summary

analgesic effect of superficial cervical plexus block by using ultrasound in patients undergoing neck surgeries

Conditions

  • Postoperative Pain

Interventions

PROCEDURE

superficial cervical plexus block guided by ultrasound with bupivacaine

in active group we will use bupivacaine in superficial cervical plexus block to deal with pain postoperative neck surgeries

DRUG

Paracetamol (500 mg) tablets

controlled group will take shame block with normal saline and paracetamol only

Sponsors & Collaborators

  • Sohag University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-03-16
Primary Completion
2027-03-30
Completion
2027-10-30
FDA Drug
Yes

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07539935 on ClinicalTrials.gov