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NCT05301634

Comparison Between Bilateral Infraorbital Block Versus Intranasal Bupivacaine in Transsphenoidal Pituitary Adenoma Resection

Completed Phase 3 Last updated 30 December 2025
What this trial tests

Phase 3 trial testing infraorbital block in Intraoperative Hypertension in 60 participants. Completed in 15 December 2025.

Timeline
2 April 2022
Primary endpoint
30 July 2025
15 December 2025

Quick facts

Lead sponsorCairo University
PhasePhase 3
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment60
Start date2 April 2022
Primary completion30 July 2025
Estimated completion15 December 2025
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Cairo University

Who can join

21 and older, any sex, with Intraoperative Hypertension. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The study will evaluate the efficacy of bilateral infraorbital nerve block versus preoperative nasal packing with long-acting local anesthetic bupivacaine in term of maintaining hemodynamics intraoperative within 20% below baseline to achieve adequate hypotensive anesthesia and longer duration of postoperative analgesia up to 24 hours in patients undergoing transsphenoidal pituitary adenoma resection.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Intraoperative Hypertension

Currently open trials in the same condition.

Other Cairo University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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