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Recruiting NCT07523438

NCT07523438 Effect of Intranasal Dexmedetomidine on the Incidence of Emergence Agitation in Children Undergoing Strabismus Surgery

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Clinical Trial Summary
NCT ID NCT07523438
Status Recruiting
Phase
Sponsor Alexandria University
Condition Dexmedetomidine
Study Type INTERVENTIONAL
Enrollment 120 participants
Start Date 2026-03-01
Primary Completion 2026-09-01

Eligibility & Interventions

Sex All sexes
Min Age 3 Years
Max Age 6 Years
Study Type INTERVENTIONAL
Interventions
high dex grouplow dex group

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 120 participants in total. It began in 2026-03-01 with a primary completion date of 2026-09-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Dexmedetomidine is a selective a-2 adrenergic agonist that provides sedative and analgesic effects. Intranasal dexmedetomidine has a slower and gradual onset compared to intravenous injection , with low incidence of nasal discomfort. Dexmedetomidine was tested at various doses and modes of administration, as well as different types of surgery and co-anesthetic drugs, as a single injection or continuous infusion. The authors have not agreed on the ideal clinical dose. The hypothesis is that intranasal dexmedetomidine 3mcg /kg will decrease the incidence of emergence agitation after strabismus surgery than dexmedetomidine 2 mcg/kg

Eligibility Criteria

Inclusion Criteria: * Age: 3-6 years, both sexes * ASA physical status class I , II. Exclusion Criteria: * history of neurological and psychiatric disease * body mass index \> 20 kg m-2 * allergy to dexmedetomidine * patients on medical treatment which has any sedative effect * mentally retarded children

Contact & Investigator

Central Contact

sarah m elgamal, MD

✉ sarahelgamal1990@yahoo.com

📞 01005496440

Principal Investigator

sarah m elgamal, MD

PRINCIPAL INVESTIGATOR

Alexandria University

Frequently Asked Questions

Who can join the NCT07523438 clinical trial?

This trial is open to participants of all sexes, aged 3 Years or older, up to 6 Years, studying Dexmedetomidine. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07523438 currently recruiting?

Yes, NCT07523438 is actively recruiting participants. Contact the research team at sarahelgamal1990@yahoo.com for enrollment information.

Where is the NCT07523438 trial being conducted?

This trial is being conducted at Alexandria, Egypt.

Who is sponsoring the NCT07523438 clinical trial?

NCT07523438 is sponsored by Alexandria University. The principal investigator is sarah m elgamal, MD at Alexandria University. The trial plans to enroll 120 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology