← Eichor
Study identifier: NCT07108764 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Intraoperative Infusion of Either Lidocaine or Dexmedetomidine on Regional Cerebral Oxygen Saturation and Postoperative Delirium in Elderly Patients Undergoing Abdominal Surgeries

Condition: Intraoperative Infusion · Lidocaine · Dexmedetomidine  ·  Sponsor: Tanta University

PhaseNA
Planned participants100
Who can joinAll sexes, 65 Years to no upper limit
Healthy volunteersNo

About this study

This study aims to compare the effect of intraoperative infusion of either lidocaine or dexmedetomidine on the incidence of postoperative delirium (POD) in elderly patients undergoing major surgeries. It also aims to evaluate the impact of both medications on intraoperative regional cerebral oxygen saturation (rSO₂).

This description comes directly from the study's public registry record.

Talk to the study team

Dina H Alhassanin, Master  ·  00201143441294  ·  dhamdy420@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Tanta UniversityTanta, El-Gharbia, EgyptRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07108764