RecruitingNot ApplicableNCT07708740

Two Intravenous Doses of Ketamine in Reducing the Oculocardiac Reflex in Adult Patients Undergoing Ophthalmic Surgery

Evaluation of Two Intravenous Doses of Ketamine in Reducing the Oculocardiac Reflex in Adult Patients Undergoing Ophthalmic Surgery: A Randomized Controlled Double-Blinded Trial


Sponsor

Cairo University

Enrollment

40 participants

Start Date

Jul 1, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

This study aims to evaluate whether a lower dose of ketamine (0.5 mg/kg IV) may be as effective as a higher dose (0.75 mg/kg IV) in reducing oculocardiac reflex (OCR) incidence in adult patients undergoing ophthalmic surgery.


Eligibility

Min Age: 18 YearsMax Age: 65 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called 0.5 mg/kg intravenous ketamine and a drug called 0.75 mg/kg intravenous ketamine for people with ketamine, oculocardiac reflex, and other related conditions. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years to 65 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUG0.5 mg/kg intravenous ketamine

Patients will receive 0.5 mg/kg intravenous ketamine hydrochloride.

DRUG0.75 mg/kg intravenous ketamine

Patients will receive 0.75 mg/kg intravenous ketamine hydrochloride.


Locations(1)

Cairo University

Cairo, Egypt

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NCT07708740


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