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Ultrasound-Guided Versus Brainlab Navigation Sphenopalatine Ganglion Block in Functional Endoscopic Sinus Surgery

T

Tanta University

Status

Completed

Conditions

Sphenopalatine Ganglion Block
Functional Endoscopic Sinus Surgery
Brainlab Navigation
Ultrasound

Treatments

Other: Low dose Brainlab navigation sphenopalatine ganglion block
Other: Brainlab navigation sphenopalatine ganglion block
Other: Ultrasound-guided sphenopalatine ganglion block

Study type

Interventional

Funder types

Other

Identifiers

NCT06984913
36264PR1183/4/25

Details and patient eligibility

About

This study compares ultrasound-guided and Brainlab navigation sphenopalatine ganglion block (SPGB) in functional endoscopic sinus surgery (FESS).

Full description

Functional endoscopic sinus surgery (FESS) is the treatment modality of choice for the inflammatory disease of paranasal sinuses.

Sphenopalatine ganglion block (SPGB) is a regional analgesic technique that can be used as an alternative approach to reduce blood loss and improve the operative field during FESS without the need for hypotensive agents.

Ultrasound (US)-guided nerve block is a well-established technique in regional anesthesia and offers the advantage of real-time visualization of neural and vascular structures.

Enrollment

60 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age from 18 to 65 years.
  • Both sexes.
  • American Society of Anesthesiologists (ASA) physical status I-II.
  • Patients undergoing functional endoscopic sinus surgery under general anesthesia.

Exclusion criteria

  • Patients having a history of severe renal, hepatic, respiratory, cardiac disease, or a neurological condition.
  • Drug or alcohol abuse.
  • Chronic pain requires major analgesics, sedatives, or corticosteroids.
  • Pregnant and lactating women.
  • Hypersensitivity to local anesthetic agents.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 3 patient groups

Ultrasound group
Experimental group
Description:
Patients will receive an ultrasound-guided sphenopalatine ganglion block (4 ml bupivacaine 0.25%).
Treatment:
Other: Ultrasound-guided sphenopalatine ganglion block
Brainlab group
Experimental group
Description:
Patients will receive a Brainlab navigation sphenopalatine ganglion block (4 ml bupivacaine 0.25%).
Treatment:
Other: Brainlab navigation sphenopalatine ganglion block
Low dose Brainlab group
Experimental group
Description:
Patients will receive a Brainlab navigation sphenopalatine ganglion block (2 ml bupivacaine 0.25%) (low dose).
Treatment:
Other: Low dose Brainlab navigation sphenopalatine ganglion block

Trial contacts and locations

1

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Central trial contact

Mostafa I Sharaf, MD

Data sourced from clinicaltrials.gov

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