COMPUFLO: Monitoring of Injection Pressure During Regional Anesthesia in Pediatric Patient

Sponsor
University Hospital, Montpellier (Other)
Overall Status
Unknown status
CT.gov ID
NCT03672526
Collaborator
(none)
150
1
1
24
6.2

Study Details

Study Description

Brief Summary

A low injection pressure is one of the safety elements to check the correct position of the needle during regional anesthesia. Subjective assessment of pressure during manual injection of local anesthetic is most commonly used. In adults, the monitoring of the injection pressure has already been evaluated and makes it possible to objectify the pressure of the injection pressure. This is possible thanks to a device named Compuflo. No study has measured injection pressures during a regional anesthesia in children. The main objective is to control the injection pressures exercised in daily clinical practice during pediatric regional anesthesia with the Compuflo. Regional anesthesia will be proposed and explained during the anesthesia consultation. The procedure will be performed according to the habits of the anesthesiologist in charge of the patient. Only the addition of the Local Anesthetic Injection Pressure monitoring (Compuflo) to the needle changes the usual setup.

Condition or Disease Intervention/Treatment Phase
  • Device: measure of injection pressure by compuflo
N/A

Detailed Description

The purpose of this study is to evaluate the usual practice using Compuflo, allowing the continuous measurement of the injection pressure of the local anesthetic at the needle level. On the day of the surgery, an anesthesiologist "operator" will realize the echo-guided regional anesthesia, qualifying aloud every injection realized (site or compartment of injection, and volume injected). An "observer" anesthesiologist will note the demographic data (age and weight), then the material data (minimum stimulation intensity, type and size of needles and syringes used), and finally he will note the maximum pressure levels reached during the injections performed.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
150 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Use of Compuflo in Pediatric Anesthesia: Monitoring of Injection Pressure of Local Anesthetics in Children
Actual Study Start Date :
Oct 8, 2018
Anticipated Primary Completion Date :
Oct 8, 2020
Anticipated Study Completion Date :
Oct 8, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: device compuflo

Device: measure of injection pressure by compuflo
injection pressure mesured by Compuflo

Outcome Measures

Primary Outcome Measures

  1. injection pressure (injection pressure measured by Compuflo) [up to 24 hours (during the ALR)]

    injection pressure measured by Compuflo

Secondary Outcome Measures

  1. Pressure values compared to the threshold value used in adults of 15 Psi [up to 24 hours (during the ALR)]

    Pressure values compared to the threshold value used in adults of 15 Psi

  2. Pressure values according to the different types of material used [up to 24 hours (during the ALR)]

    Pressure values according to the different types of material used

  3. Pressure values in the different infiltrated compartments [up to 24 hours (during the ALR)]

    Pressure values in the different infiltrated compartments

  4. Pressure values according to the age of the child [up to 24 hours (during the ALR)]

    Pressure values according to the age of the child

  5. Number and ratio of involuntary intra-neural injections [up to 24 hours (during the ALR)]

    Number and ratio of involuntary intra-neural injections

  6. Number and ratio of secondary paresthesias [up to 24 hours (during the ALR)]

    Number and ratio of secondary paresthesias

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A to 16 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Minor patient (0-16 years old) with consent of the major legal representative

  • Affiliated to the social security

  • Informed written consent, notification on the anesthesia sheet

Exclusion Criteria:
  • Patient over 16 years old

  • Patient under tutorship / curatorship

  • Young girl with known or suspected ongoing pregnancy

  • Known allergy to local anesthetics

  • Hemostatic disorder

  • Local infection at the puncture site

Contacts and Locations

Locations

Site City State Country Postal Code
1 University Hospital of Montpellier Montpellier France 34380

Sponsors and Collaborators

  • University Hospital, Montpellier

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Hospital, Montpellier
ClinicalTrials.gov Identifier:
NCT03672526
Other Study ID Numbers:
  • RECHMPL17_0399
First Posted:
Sep 14, 2018
Last Update Posted:
Aug 27, 2020
Last Verified:
Aug 1, 2020
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Aug 27, 2020