Study of the Efficacy of Moderate Sedation With Intra-NAsal Dexmedetomidine Monitored by EEG MOnitoring

NCT06867289 — Not applicable, Recruiting, 50 participants, Centre Hospitalier Régional Metz-Thionville

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RegistryNCT06867289, acronym DINAMO
StatusRecruiting
PhaseNot applicable
Study typeInterventional; na, single group, masking: none, diagnostic
Enrollment50 (Estimated)
SponsorCentre Hospitalier Régional Metz-Thionville (Other)
ConditionsProcedural Sedation and Analgesia, Pediatric ALL
InterventionsEEG (Device)
Datesstart 2025-04-08, primary completion 2027-04-08 (estimated), completion 2027-04-08 (estimated), first posted 2025-03-10, last updated 2026-03-12
Locations1 site in France

Related Papers Related Patents Related Grants Related Experts
All trials for Procedural Sedation and Analgesia All trials for Pediatric ALL All trials of EEG

-Summary

This is a prospective, monocentric diagnostic study aiming to evaluate whether a sedation score obtained by a per-procedural electroencephalogram (EEG), the PSI score, could identify patients for whom a 2 μg/kg dose of DEX would not be sufficient for the successful performance of cerebral NMRI, and who could therefore benefit from a higher dosage of DEX (4 μg/kg).

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+Detailed description

For some children, brain MRI is a particularly important examination for etiological assessment or for monitoring the progress of neurological diseases. It can sometimes be complicated to perform, due to the age and/or pathology of the child concerned. Impossibility, postponement or the need for a general anaesthetic are constraints that should be avoided as far as possible. Procedural sedation with dexmedetomidine (DEX) can be administered intra-nasally. This technique offers good results and safety of use. Nevertheless, the failure rate is 20% to 30%, and may depend on the dosage of DEX used (indicated doses vary from 2 to 4 μg/kg). This study aims to evaluate whether a sedation score obtained by a per-procedural electroencephalogram (EEG), the PSI score, could identify patients for whom a 2 μg/kg dose of DEX would not be sufficient for the successful performance of cerebral NMRI, and who could therefore benefit from a higher dosage of DEX (4 μg/kg).

+Arms and interventions

ArmTypeInterventionsDescription
EEG Monitoring and PSSS clinical scoreExperimentalDevice: EEGAll participants receive an EEG monitoring.
  • EEG (Device): EEG monitoring will be performed in addition to the usual practice, before DEX administration and for 20 minutes before NMRI, to enable calculation of the PSI sedation score (at 0, 10, 20 minutes). Sedation will also be assessed by the PSSS clinical score at 0, 10, 20 minutes after DEX administration, as well as at 150 minutes after DEX.

+Outcome measures

Primary outcomes

  • Prediction of complete NMRI success [20 minutes after DEX administration]: To describe the predictive value (ROC curve) of the PSI score assessed 20 minutes after administration of 2 μg/kg of DEX intranasally, for complete success in performing brain NMRI in children under 5 years of age, or over 5 years of age with risk of failure. Successful NMRI is defined as: * Complete if all prescribed sequences can be interpreted without reservation, * Partial if some of the sequences cannot be interpreted or are subject to reservations by the radiologist, * Absent if the examination is cancelled or if all sequences are uninterpretable or subject to reservations. PSI score: evaluated on EEG, the score varies from 0 to 100.

Secondary outcomes

  • Complete or partial success in performing brain NMRI in children under 5 years of age, or over 5 years of age with risk of failure. [20 minutes after DEX administration]: Area under the ROC curve for prediction of complete or partial success of NMRI according to PSI score. Successful NMRI is defined as: * Complete if all prescribed sequences can be interpreted without reservation, * Partial if some of the sequences cannot be interpreted or are subject to reservations by the radiologist, * Absent if the examination is cancelled or if all sequences are uninterpretable or subject to reservations.
  • Predictive value (ROC curve) of the PSI score for successful completion of brain MRI in children under 5 years of age, or over 5 years of age with risk of failure. [20 min after DEX administration]: Area under the ROC curve for prediction of complete success of NMRI according to PSI score by patient age under or over 5 years old Successful NMRI is defined as: * Complete if all prescribed sequences can be interpreted without reservation, * Partial if some of the sequences cannot be interpreted or are subject to reservations by the radiologist, * Absent if the examination is cancelled or if all sequences are uninterpretable or subject to reservations. PSI score: evaluated on EEG, the score varies from 0 to 100.
  • Predictive value (ROC curve) of the PSSS score for successful completion of brain MRI in children under 5 years of age, or over 5 years of age with risk of failure. [20 min after DEX administration]: Area under the ROC curve for prediction of complete or partial success of NMRI according to PSSS score at 20 minutes Successful NMRI is defined as: * Complete if all prescribed sequences can be interpreted without reservation, * Partial if some of the sequences cannot be interpreted or are subject to reservations by the radiologist, * Absent if the examination is cancelled or if all sequences are uninterpretable or subject to reservations. PSSS score: ranges from 0 (deepest sedation) to 5 (shallowest sedation) depending on the observation of clinical signs in children
  • Correlation between PSI and PSSS scores [at 0, 10, 20 and 150 minutes after DEX administration]: Describe the correlation between PSI score and PSSS score PSI scores at 0, 10, 20 and 150 minutes after DEX administration and PSSS scores at 0, 10, 20 and 150 minutes after DEX administration
  • Complications (Quality of recovery) [at 150 minutes after DEX administration]: PSSS score: ranges from 0 (deepest sedation) to 5 (shallowest sedation) depending on the observation of clinical signs in children
  • Complications (Blood Pressure) [at 0, 10, 20 and 150 minutes after DEX administration]: mmHg
  • Complications (Heart Rate) [at 0, 10, 20 and 150 minutes after DEX administration]: bpm
  • Complications (Oxygen Saturation) [at 0, 10, 20 and 150 minutes after DEX administration]: SaO2 (%)
  • Complications (allergic reactions) [at 0, 10, 20 and 150 minutes after DEX administration]: number and types

+Eligibility

Sex: All, ages: 1 Year to 18 Years

Inclusion Criteria:

* Indication of DEX sedation for brain NMRI at the CHR de Metz-Thionville

  * in a patient aged between 12 months and 5 years or
  * for a patient aged between 5 and 18 whose cooperation during the examination appears compromised (previous failure, autism spectrum disorders, etc.).
* Membership of a social security scheme
* Free and informed consent obtained from the patient's legal guardian(s).

Exclusion Criteria:

* Weight < 10 kg
* Patients with contraindications to the use of DEX

  * Hypersensitivity to the active ingredient or to any of the excipients listed in the section on "Hypersensitivity".
  * Advanced heart block (level 2 or 3), unless pacemaker implanted
  * Uncontrolled hypotension
  * Acute cerebrovascular pathologies
* Patients with nasal obstruction
* Parental refusal of DEX administration
* Minors under guardianship
* Minors under judicial sanction

+Locations (1)

FacilityCityCountryStatus
CHR Metz-Thionville Hopital Femme-Mère EnfantMetzFranceRecruiting

+Investigators

  • Anne-Charlotte CULLIER, MD, Principal investigator, CHR Metz Thionville Hopital Femme Mère Enfant