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Comparison of Dexmedetomidine and Midazolam for Intra-op Sedation in TIVA in Children Undergoing Inguinal Hernia Repair

To Compare Dexmedetomidine and Midazolam for Intra-op Sedation in TIVA in Children Undergoing Inguinal Hernia Repair

Status
UNKNOWN
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05337085
Enrollment
185
Registered
2022-04-20
Start date
2022-06-30
Completion date
2023-03-20
Last updated
2022-04-20

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

Conditions

Inguinal Hernia

Brief summary

To compare dexmedetomidine and midazolam for intra-op sedation in TIVA in children undergoing inguinal hernia repair. The results of the study if found significant will guide the anesthetist in appropriate choice and dose of sedative drug with highest efficacy and minimum side effects to avoid post operative adverse effects associated with anesthesia

Interventions

DRUGDexmedetomidine

Inj dexmedetomidine and inj midazolam given to 2 groups of participants and sedative effects of both drugs will be observed during surgery

DRUGMidazolam

Midazolam

Sponsors

Sheikh Zayed Medical College
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
12 Months to 15 Years
Healthy volunteers
Yes

Inclusion criteria

* Male and female paediatric patients In age range neonates to 15 years * Planned for elective inguinal hernia repair * Patients with uncomplicated hernia With ASA class I or II

Exclusion criteria

* Patients undergoing emergency inguinal repair * Patients with ASA class III,IV,V or VI * Patients present with complicated hernia * Patients with BMI above 40kg/m2 * Patients with any allergy to anesthesia * Patients with coagulopathy * Patients with narcotic/opioid addiction

Design outcomes

Primary

MeasureTime frame
Level of sedation assessed through Ramsay Sedation Scale RSS6 months

Contacts

Primary ContactAnab Farooqi, MBBS
zaibanaab94@gmail.com03337923232

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026