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Search / Trial NCT02505646

Fluid Responsiveness Evaluation by AbdomiNal Compression in Kids Based on the STARLING Concept

Launched by HOPITAL LOUIS PRADEL · Jul 21, 2015

Trial Information

Current as of June 02, 2025

Completed

Keywords

Circulatory Failure Fluid Responsiveness Abdominal Compression

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Age \< 8 years old
  • * Patient with a circulatory failure defined as follow :
  • Treatment including vasopressor or inotrope
  • OR macrocirculatory failure
  • Heart rate \> 2 Standard Deviation (SD)
  • Systolic arterial pressure \< 2 SD
  • Mean arterial pressure \< 2 SD
  • Diastolic arterial pressure \< 2 SD
  • WITH signs of microcirculatory failure
  • Capillary refill time \> 2 secondes
  • Blotch
  • Organ dysfunction due to the circulatory failure (Oliguria \< 0,5 ml/kg/h, acute lung injury, encephalopathy)
  • Exclusion Criteria:
  • Opposition from the parents or the one who holds the parental authority
  • Cardiogenic acute pulmonary edema,
  • Extreme hemodynamic instability,
  • Intra-abdominal hypertension,
  • Recent abdominal surgery that does not permit an abdominal compression without causing pain.
  • Patient with mechanical circulatory support, such as Extra Corporal Life Support or Berlin-Heart
  • Patient with congenital cardiopathy with a palliative correction or an incomplete correction
  • Open thorax
  • Prone position
  • Investigators not available
  • No security number registration.
  • Moribund patient

About Hopital Louis Pradel

Hospital Louis Pradel is a renowned healthcare institution specializing in cardiovascular and metabolic diseases, dedicated to advancing medical research and improving patient outcomes. With a strong commitment to innovation, the hospital actively conducts clinical trials aimed at evaluating new therapeutic interventions and medical technologies. Backed by a team of experienced researchers and healthcare professionals, Hospital Louis Pradel fosters a collaborative environment that prioritizes patient safety and ethical standards, ensuring that all trials contribute valuable insights to the medical community and enhance the quality of care provided to patients.

Locations

Lyon, , France

Lyon, , France

Patients applied

0 patients applied

Trial Officials

Jean-Luc Fellahi, MD, PhD

Study Director

Hôpital Louis Pradel, Hospice Civil de Lyon

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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