- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT03283865
Does Use of Ultrasound Reduce the Rate of Sham Caudal Block in Children
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
Caudal blocks are one of the most commonly performed regional anesthetics in children and are performed daily for a host of infra-umbilical surgical procedures. A caudal block is an epidural injection, most commonly of local anesthetic into the epidural space as accessed via the sacral hiatus. In children, the sacral hiatus is a normally occurring aperture in which the epidural space may be accessed with extremely minimal risk; as neural tissue ends more proximally. Due to this measure of safety, caudal blocks are preferred in children when compared with standard lumbar epidurals. Caudal blocks are performed blindly using palpation and tactile feedback to assess if the medication is being administered in the correct location. As a result of blind injection, administration of local anesthetic totally or partially outside of the correct site can often be unnoticed or identified after a significant volume has already been injected. With the potential for toxicity of local anesthetic, this may result in either the inability to give a complete dose or an unintentional and often unnoticed sham block "incorrect site of injection".
Use of ultrasound has been proposed for identification of caudal block placement and correct medication spread. However, a recent review of the Pediatric Regional Anesthesia Network database reveals that ultrasound is reportedly only used in less that 3% of blocks. The benefit of ultrasound is safe and real-time confirmation of injection. Ultrasound allows the provider to determine with minimal local anesthetic or even saline injection if the correct space is accessed. Without ultrasound, failed blocks are either identified after significant percentage of the total dose of local anesthetic is incorrectly administered or intra or post operatively when the patient demonstrates a significant opioid requirement. This is problematic given that one of the primary benefits of a caudal block in children is the ability to avoid opioids.
Review of local practice here at Texas Children's Hospital for quality improvement purposes revealed a failure rate of caudal blocks to be 18%. Failure was defined as a heart rate increase with incision of >20% despite a caudal block and >1MAC of gas for the patient age. These patients all required opioids both intra and post operatively in addition to surgical levels of inhaled anesthetic agent.
Type d'étude
Phase
- N'est pas applicable
Contacts et emplacements
Lieux d'étude
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Texas
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Houston, Texas, États-Unis, 77030
- Texas Childrens Hospital
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Inclusion Criteria:
- Children ages 0-84 months
- Infra-umbilical procedure for which a caudal block is already planned
- American Society of Anesthesiology classifications of 1,2 or 3
Exclusion Criteria:
- Incarcerated hernias
- Emergency procedures
- Local Anesthetic allergy
- Sacral dimple
- Rash over sacrum
- Parents/legal guardians unable to consent for surgical procedure in English language Foster Care/Child protective services as guardians
- Parental Refusal for caudal block or study participation
- American Society of Anesthesiology classifications other than 1,2 or 3
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: N / A
- Modèle interventionnel: Affectation à un seul groupe
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
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Expérimental: Ultrasound
The attending anesthesiologist will perform or instruct the placement of a caudal block according to their standard of practice. At the time of administration of local anesthetic into the caudal space, the study collaborator (SC) will ultrasound the caudal space keeping the provider placing the block blinded to the imaging. The provider placing the block will inject 0.5mL of saline. The provider will then be asked to state if they are correctly in the caudal space or not. If the provider feels they are not in the caudal space, they will re-do the procedure. If the provider fails to identify incorrect location and this is noted by ultrasound, the SC will inform the provider to re-do the procedure. All study participants will have ultrasound used for caudal block. |
The attending anesthesiologist will perform or instruct the placement of a caudal block according to their standard of practice.
At the time of administration of local anesthetic into the caudal space, the study collaborator (SC) will ultrasound the caudal space keeping the provider placing the block blinded to the imaging.
The provider placing the block will inject 0.5mL of preservative free saline.
The provider will then be asked to state if they are correctly in the caudal space or not.
If the provider feels they are not in the caudal space, they will re-do the procedure.
If the provider fails to identify incorrect location and this is noted by ultrasound, the SC will inform the provider to re-do the procedure
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Identify the rate at which blindly placed caudal blocks are not within the epidural space
Délai: 15 minutes
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Assess the percentage of providers not recognizing wrong site of injection without ultrasound
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15 minutes
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Identify the rate at which ultrasound can guide a wrong block into the correct location
Délai: 15 minutes
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Assess the number of blocks that are require the use of ultrasound to redirect needle into caudal space
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15 minutes
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Identify if lack of heart rate change on incision can predict successful placement when medication administration is successfully confirmed with ultrasound
Délai: 15 minutes
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With ultrasound identification of correct caudal injection, (successful block), does lack of heart rate change correlated with successful block
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15 minutes
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Identify if after using ultrasound to visualize placement, if concentrations of inhaled agents may be reduced in children
Délai: 30 minutes to 3 hours
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With demonstration of successful caudal injection, can inhaled agent concentration be reduced as calculated by MAC hours
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30 minutes to 3 hours
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Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Chercheur principal: Adam C Adler, MD, FAAP, Texas Childrens Hospital
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Autres numéros d'identification d'étude
- H-40844
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Informations sur les médicaments et les dispositifs, documents d'étude
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Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .
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