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Not yet recruiting NCT07555821

Improving Postoperative Analgesia After Functional Endoscopic Surgery

Phase II / Phase III Interventional Pain Management After Functional Endoscopic Sinuscopy

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Sphenopalatine ganglion block (SPGB) with Bupivacaine and Dexmedetomidine.
Who it may be relevant to
Registry conditions: Pain Management After Functional Endoscopic Sinuscopy. Basic parameters: 18 years — 60 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Improving Postoperative Analgesia After Functional Endoscopic Surgery: Sphenopalatine Ganglion Block Versus Soaked Nasal Packing Using Bupivacaine and Dexmedetomidine

Overview

Improving postoperative analgesia after functional endoscopic surgery: Sphenopalatine ganglion block versus soaked nasal packing using bupivacaine and dexmedetomidine

Interventions

  • Drug Sphenopalatine ganglion block (SPGB) with Bupivacaine and Dexmedetomidine
    Sphenopalatine ganglion block (SPGB) with Bupivacaine and Dexmedetomidine

Primary outcome measures

  • effectiveness of SPGB with bupivacaine and dexmedetomidine for postoperative analgesia [Time frame: 6 months]

Eligibility criteria

Inclusion criteria

  • Age 18 - 60 years
  • ASA physical status I -II
  • Patients scheduled for elective FESS

Exclusion criteria

  • Allergy to drugs used
  • Coagulopathy or anticoagulant therapy
  • Severe cardiovascular, renal and hepatic disease
  • Chronic opioid use Pregnancy

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Factorial
Masking
Quadruple blind
Primary purpose
Supportive care

Study locations

Egypt · 1 center
  • Assiut university hospital — Asyut

Identifiers

NCT: NCT07555821 · 04-2026-300806

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗