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Clinical Trials in Egypt / NCT07555821
Starting soon Phase 2/3

Improving Postoperative Analgesia After Functional Endoscopic Surgery

NCT07555821 · tracked via the Priya Life Science Egypt tracker
Sponsor
South Egypt Cancer Institute
Phase
Phase 2/3
Started
2026-04-15
Last updated
2026-04-29

Condition(s) studied

Pain Management After Functional Endoscopic Sinuscopy

Investigational drug(s) / intervention(s)

Sphenopalatine ganglion block (SPGB) with Bupivacaine and Dexmedetomidine

Sphenopalatine ganglion block (SPGB) with Bupivacaine and Dexmedetomidine: Sphenopalatine ganglion block (SPGB) with Bupivacaine and Dexmedetomidine

Study summary

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

Eligibility

Sex
ALL
Min age
18 Years
Max age
60 Years
Healthy volunteers
No
Inclusion Criteria: 1. Age 18 - 60 years 2. ASA physical status I -II 3. Patients scheduled for elective FESS Exclusion Criteria: 1. Allergy to drugs used 2. Coagulopathy or anticoagulant therapy 3. Severe cardiovascular, renal and hepatic disease 4. Chronic opioid use Pregnancy

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Assiut university hospital Asyut Egypt

More South Egypt Cancer Institute trials in Egypt

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07555821 on ClinicalTrials.gov ↗ ← All trials in Egypt