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Recruiting NCT05566431

Benchmark Evidence Led by Latin America: Trial of Intracranial Pressure - Pediatrics

No phase Interventional Severe Traumatic Brain Injury

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: ICP, CREVICE.
Who it may be relevant to
Registry conditions: Severe Traumatic Brain Injury. Basic parameters: 1 year — 12 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States, Colombia, El Salvador, Guatemala, Honduras +1
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Pediatric Severe Traumatic Brain Injury in Latin America - A Randomized Trial Comparing Two Management Protocols

Overview

Narrative: Worldwide, traumatic brain injury (TBI) is a leading cause of death and disability among children and adolescents. The Investigators aim to test whether pediatric TBI treatment guided by invasive intracranial pressure monitoring produces better patient outcomes than care guided by a protocol without invasive monitoring. Study findings will inform clinical practice in treating pediatric severe TBI globally. Focused didactic and experience-based learning opportunities will increase the research capacity of pediatric intensivists in Latin America.

Detailed description

Abstract:

Children who survive severe traumatic brain injury (sTBI) live with profound impairments that alter their development and future possibilities. Worldwide, TBI is the leading cause of death and disability for children/ adolescents with the US annual incidence 6 times greater than MS, HIV/AIDS, spinal cord injury, and breast cancer combined.

Our primary focus for scientific investigation is to conduct a high quality randomized controlled trial addressing a critical TBI management question: Does using a protocol with information from intracranial pressure (ICP) monitoring to direct treatment of children with sTBI improve outcomes vs an aggressive management protocol based on imaging and clinical examination alone? This follows on our adult ICP study which found no outcome differences and has occasioned re-thinking of treatment guidelines for sTBI patients \>13. A separate study is essential because children are not simply small adults and some treatment approaches carry age-related additional risks. Thus, study findings will inform US and global clinical practice.

This trial will be conducted in 8 Latin American pediatric ICUs where infrastructures and practice patterns are optimal for strong internal validity and resources represent trauma care in the developing world. The successful adolescent/adult BEST TRIP trial, which collected high-quality data in similar environments (cited \> 900 times) underscores the feasibility of this approach.

Specific Aim: In a Phase III randomized superiority trial in 428 children with sTBI from 8 Latin American pediatric trauma centers, test the effect on outcomes of management of sTBI guided by a protocol using information from ICP monitors vs. management using a protocol that uses imaging and clinical exams to guide treatment.

Hypothesis #1: Children with severe TBI whose acute care treatment is managed using a protocol based on data from ICP monitoring will have significantly lower mortality and better quality of life and global outcome at 6 months post-trauma than those whose treatment is managed with a protocol based on imaging and clinical exam. The primary measure of functional recovery is the PedsQL at 6 months. A secondary measure is GOSE-Peds.

Hypothesis #2: Incorporating ICP monitoring into sTBI patient care will minimize secondary complications, decrease length of stay in ICU and decrease brain-specific treatments.

Specific Aim: The Investigators will train personnel in centers new to research how to conduct high-quality scientific studies, and will extend the training for the personnel with whom the Investigators have been working, solidifying previous capacity-building efforts, and initiating new efforts.

Interventions

  • Other ICP
    The intervention is a management protocol that includes ICP monitoring for children with severe traumatic brain injury
  • Other CREVICE
    The intervention is a management protocol that is based on imaging and clinical examinations without ICP monitoring for children with severe traumatic brain injury

Primary outcome measures

  • Pediatric Quality of Life Inventory (PedsQL) [Time frame: 6 months after injury]
Secondary outcome measures (5)
  • Pediatric Quality of Life Inventory (PedsQL) [Time frame: 3 months after injury]
  • Glasgow Outcome Scale - Extended (GOS-E) Pediatric [Time frame: 3 and 6 months after injury]
  • Mortality [Time frame: 3 and 6 months]
  • Brain-specific interventions [Time frame: 1 month average]
  • ICU length of stay [Time frame: 1 month average]

Eligibility criteria

Inclusion criteria

  • Provision of signed and dated informed consent form by the parent(s) or guardian(s)
  • Non-penetrating TBI
  • Admission to study hospital within 24 hours of injury
  • Total GCS score ≤ 8 on admission or within first 48 hours after injury (measured using pediatric GCS 1 for children < 2 years old and standard GCS for older children)
  • Age 1 through 12 years
  • Able to randomize:
  • Within 24 hours of injury (for patients with GCS ≤ 8 on admission) OR
  • Within 24 hours of deterioration (for patients deteriorating to GCS ≤ 8 within 48 hours of injury)

Exclusion criteria

  • Motor GCS score of 6
  • GCS of 3 with bilaterally fixed and dilated pupils
  • Injury thought to be intentionally inflicted by a family member or caregiver.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Treatment

Study locations

Guatemala · 3 centers
  • Hospital Regional de Esquintla — Escuintla
  • Hospital General San Juan de Dios — Guatemala City
  • Hospital Regional de Occidente San Juan de Dios — Quetzaltenango
Peru · 3 centers
  • Hospital de Emergencias Pediátricas — Lima
  • Hospital Edgardo Rebagliati Martins — Lima
  • Instituto Nacional de Salud del Niño - San Borja — Lima
Colombia · 2 centers
  • Fundación Hospital de la Misericordia — Bogotá
  • Hospital Fundacion Amigos de la Salud — Montería
United States · 1 center
  • University of Washington, Harborview Medical Center — Seattle
El Salvador · 1 center
  • Hospital de Niños Benjamín Bloom — San Salvador
Honduras · 1 center
  • Hospital Escuela — Tegucigalpa

Publications

  • Chesnut R, Temkin N, Pridgeon J, Sulzbacher S, Lujan S, Videtta W, Moya-Barquin L, Chaddock K, Bonow RH, Petroni G, Guadagnoli N, Hendrickson P, Ramirez Cortez G, Carreazo NY, Vargas Aymituma A, Anchante D, Caqui P, Ramirez A, Munaico Abanto M, Ortiz Chicchon M, Cenzano Ramos J, Castro Darce MDC, Sierra Morales R, Brol Lopez P, Menendez W, Posadas Gutierrez S, Kevin V, Mazariegos A, de Leon E, Rod PMID 37955439
  • Chesnut R, Temkin N, Pridgeon J, Sulzbacher S, Lujan S, Videtta W, Moya-Barquin L, Chaddock K, Bonow R, Petroni G, Guadagnoli N, Hendrickson P, Ramirez Cortez G, Carreazo NY, Vargas Aymituma A, Anchante D, Caqui P, Ramirez A, Munaico Abanto M, Ortiz Chicchon M, Cenzano Ramos J, Mazate-Mazariegos A, Castro Darce MDC, Sierra Morales R, Brol Lopez P, Menendez W, Posadas Gutierrez S, Kevin V, Mazarieg PMID 37409817

Identifiers

NCT: NCT05566431 · STUDY00013122 · 1R01HD106273-01

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗