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Investigating the effect of nasal dexmedetomidine and midazolam in children undergoing neurosurgery on anxiety before and and pain levels after surgery.

Investigating the effect of nasal dexmedetomidine and midazolam in children undergoing neurosurgery on anxiety before and and pain levels after surgery.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200518047491N2
Enrollment
25
Registered
2025-04-07
Start date
2024-03-20
Completion date
Unknown
Last updated
2025-07-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pre-operative and post-operative levels of anxiety and pain.".

Interventions

Intervention 1: Intervention group:In the dexmedetomidine (DEX) group, patients received 2 mcg/kg of intranasal dexmedetomidine diluted with sterile water to a total volume of 2 cc in an unlabeled syr

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 18 Years

Inclusion criteria

Inclusion criteria: Children undergoing Neurosurgery

Exclusion criteria

Exclusion criteria: Parents didn’t agree to participate Patients ASA class 3 & 4

Design outcomes

Primary

MeasureTime frame
In comparison to midazolam, dexmedetomidine demonstrated superior efficacy in managing postoperative emergence agitation in pediatric patients. We recommend conducting further studies to investigate the advantages and disadvantages of dexmedetomidine and to compare its efficacy with other sedative agents. Timepoint: Before and After induction of anesthesia and after surgery. Method of measurement: questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNastaran Sadat Mahdavi

Shahid Beheshti University of Medical Sciences

nasimahdavi@sbmu.ac.ir+98 21 2222 7021

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026