- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07612644
Hemorrhage Elimination During Lumbar Puncture Using Ultrasound Measurements (HELPUS) (HELP)
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
Lumbar puncture (LP) is a frequently performed procedure in pediatric emergency departments, most often to evaluate meningitis in hyperthermic, hypothermic, or ill-appearing neonates, infants and children. Older children often present with headaches, meningismus, and/or altered mental status.
The risks of LP include introduction of pathogens, pain, the need for multiple attempts, and failure to obtain interpretable CSF. The latter frequently leads to a spine ultrasound study the following day and, if this does not demonstrate an epidural blood clot, repeat lumbar puncture using fluoroscopic guidance by interventional radiologists.
In evaluating the management of infant sepsis, one study found that the success of the initial LP plays a significant role: infants with unsuccessful initial LPs have longer hospital stays and require more resources. Therefore, ensuring successful LPs on the first attempt is critical for minimizing healthcare utilization, optimizing patient care, and decreasing the emotional burden of this procedure on parents and patients.
Unfortunately, epidural hematoma (EDH) is not uncommon after LP, with U/S diagnosed EDH identified among 40% of patients < 6 months with a traumatic LP and among 31% of unsuccessful but nontraumatic LP's, with complete effacement of the thecal sac in 17%. The spinal canal is wide enough to accommodate EDH with only rare sequelae. However, intramedullary hemorrhage of the conus medullaris resulting in paraplegia in a neonate has been reported.
Since the introduction of the revised febrile neonate guidelines in 2021,4 the number of lumbar punctures performed in young infants has decreased substantially. A consequence of performing fewer lumbar punctures is that clinicians-particularly trainees and early-career practitioners-have fewer opportunities to maintain procedural competence. As procedural skill and confidence decline, the risk of obtaining non-interpretable or traumatic samples increases.
Clearly, improvement of the traditional approach to LP in neonates and infants and young children is needed to prevent these complications. Ultrasound is an imaging modality that is frequently used in the emergency department and does not involve ionizing radiation. Ultrasound can be used prior to lumbar punctures to identify critical anatomical landmarks and needle-insertion distances to avoid the posterior epidural venous plexus and to increase the proportion of LP's with non-traumatic, interpretable CSF. However, an ultrasound technique that is easily learned and that can be applied accurately and efficiently in the emergency department is lacking. Incorporating ultrasound (U/S) into LP training or performance may help clinicians who perform the procedure infrequently to improve success rates and obtain interpretable cerebrospinal fluid samples through identifying optimal intervertebral spaces, visualizing spinal anatomy, and guiding needle placement.
This study employs a standardized, ultrasound-assisted LP approach that integrates pre-procedural identification of spinal anatomy and measurement of the optimal needle insertion distance along the angled trajectory to potentially minimize traumatic taps. Unlike traditional LP methods, this approach provides objective, reproducible guidance that can be given and applied by clinicians. The study is novel in its prospective assessment of ultrasound-guided LP outcomes. By evaluating interpretable CSF yield, this research advances pediatric procedural methodology and has the potential to establish a new standard of care for LP in young infants.
The overarching aim of this research is to determine whether U/S-assisted LP increases the rate of interpretable CSF from the current, approximately 65% to at least 80%.
Primary Aim: To determine the extent to which ultrasound-assisted lumbar puncture using a standardized procedure, including use of ultrasound to ascertain the presence of cerebrospinal fluid (CSF) at L3 - L5 and the optimal needle insertion distance, increases the acquisition rate of CSF that is interpretable for patient management.
Hypothesis: The standardized, ultrasound-assisted procedure for lumbar puncture in neonates and infants is associated with yield of interpretable CSF of at least 85%.
A Sufficient U/S study includes visualization of the following with each reported by the proceduralist on the data report form:
- Lower lumbar and S1 spinous processes visualized
- S1 drop-off
- L4-5 and/or L3-5 interspaces visualized
- Presence of CSF sufficient for LP
- Cauda Equina
Inclusion of lumbar punctures for which U/S was not performed:
We will review and record the results of studies performed without U/S guidance, the technique used by clinicians not participating in this study provide a prospectively acquired control group with which to compare outcomes after U/S measurement. This data will be used in the multivariable regression models described below.
Use of Previously Obtained Ultrasound Images:
As part of this study, investigators may utilize ultrasound images that were obtained as part of routine clinical care prior to the performance of lumbar puncture. These ultrasound images will have been acquired independently of, and prior to, study enrollment and will not require any additional imaging procedures for research purposes. When used for research analysis, ultrasound images will be limited to those relevant to the study objectives. Images will be accessed only by authorized study personnel and will be de-identified prior to analysis whenever feasible. No additional risk to participants is anticipated as a result of using these previously obtained clinical images.
Tipo di studio
Iscrizione (Stimato)
Fase
- Non applicabile
Contatti e Sedi
Contatto studio
- Nome: Donald H Arnold, MD, MPH
- Numero di telefono: 615-936-4498
- Email: don.arnold@vumc.org
Luoghi di studio
-
-
Tennessee
-
Nashville, Tennessee, Stati Uniti, 37232
- Reclutamento
- Vanderbilt University Medical Center
-
Contatto:
- Donald H Arnold, MD, MPH
- Numero di telefono: 615-936-4498
- Email: don.arnold@vumc.org
-
Contatto:
- Email: don.arnold@vumc.org
-
-
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
- Bambino
Accetta volontari sani
Descrizione
Inclusion Criteria:
- - Neonates and infants (< 12 months)
- Hemodynamically stable
- Undergoing a lumbar puncture for diagnostic testing
Exclusion Criteria:
- - Infants > 12 months and 1 day
- Signs of clinical instability
- Known spinal anomalies (e.g., spina bifida, meningomyelocele) or previous spinal surgery
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Diagnostico
- Assegnazione: Non randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Sperimentale: Ultrasound
Intervention: Ultrasound of spinal canal
|
Ultrasound of spinal canal without contrast.
We included the term "ultrasound contrast" because the choices were limited.
|
|
Nessun intervento: Control Group
Infants undergoing lumbar puncture without ultrasound assist
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Successful LP rate
Lasso di tempo: Time from lumbar puncture to results of CSF returned by lab, approximately 1 hour.
|
Acquisition of CSF sufficient for cell count, culture and meningoencephalitis PCR panel (MEP).
|
Time from lumbar puncture to results of CSF returned by lab, approximately 1 hour.
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Unsuccessful ultrasound attempt
Lasso di tempo: Immediately after intervention
|
Ultrasound attempt in which the ultrasound operator could not complete the study and, as a result, did not attempt to use ultrasound images to inform LP.
Potential causes include but are not limited to infant fussiness, inability to maintain positioning sufficient for ultrasound, and malfunction of the ultrasound machine.
|
Immediately after intervention
|
|
Traumatic LP rate
Lasso di tempo: Time from lumbar puncture to results of CSF returned by lab, approximately 1 hour
|
CSF RBC count > 500 cells/mm, the most widely accepted definition of traumatic LP. 10-12 The rate of traumatic LPs using this definition is 35 - 47% in neonates and 22 - 26% in infants (< 13 months).
|
Time from lumbar puncture to results of CSF returned by lab, approximately 1 hour
|
|
Number of attempts/ Number of Fluoroscopy-guided lumbar puncture (LP)
Lasso di tempo: Immediately after intervention
|
Number of attempts required for CSF acquisition or need for fluoroscopy-guided LP
|
Immediately after intervention
|
Collaboratori e investigatori
Studiare le date dei record
Studia le date principali
Inizio studio (Effettivo)
Completamento primario (Stimato)
Completamento dello studio (Stimato)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- IRB #251901 HELP Study
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
Descrizione del piano IPD
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
prodotto fabbricato ed esportato dagli Stati Uniti
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
Prove cliniche su ultrasound contrast
-
Medical University of South CarolinaSouth Carolina Spinal Cord Injury Research FundCompletatoMalattie del midollo spinale | Stenosi spinale | Lesioni del midollo spinale | Degenerazione della colonna vertebrale | Compressione del midollo spinale | Malattia della colonna vertebrale | Lesione alla colonna vertebraleStati Uniti
-
Assiut UniversityNon ancora reclutamentoLassità vaginale
-
Duke UniversityPiedmont Orthopedic SocietyCompletatoLesioni della cuffia dei rotatori | Lacerazioni della cuffia dei rotatori | Protesi totale di spallaStati Uniti
-
Association Pro-arteAttivo, non reclutanteDebolezza, Muscolo | AmiotrofiaFrancia
-
Smart Alfa Teknoloji San. ve Tic. A.S.CompletatoImaging ad ultrasuoni delle strutture anatomicheStati Uniti
-
Children's Hospital Medical Center, CincinnatiCompletatoMalattie infiammatorie intestinaliStati Uniti
-
Virginia Commonwealth UniversityGuerbetRitiratoDisfunsione dell'arteria coronaria | Danno renale acuto | Intervento coronarico percutaneoStati Uniti
-
Aga Khan UniversityNon ancora reclutamento
-
Sarasota Memorial Health Care SystemIscrizione su invitoNodulo tiroideo | Noduli tiroideiStati Uniti
-
Medical Centre LeeuwardenUniversity of Groningen; LIMIS DevelopmentReclutamento