Validation of a Capillary Leak Index During Septic Shock, Based on Haemoglobin Level Variations Induced by Fluid Resuscitation. A Pilot Study. (NCT07733206)
๐ฉบ Plain-English Summary (8th-Grade Level)
This study aims to validate a simple and reproducible index of capillary leak (CLI) in septic shock, based on haemoglobin (Hb) variation induced by standardised fluid resuscitation. To achieve this, the correlation between CLI and biomarkers of endothelial dysfunction-angiopoietin-2 and syndecan-1-will be assessed in both septic and non-septic shock patients. CLI may contribute to the individualisation of fluid management in patients with septic shock.
Who can join: Review the eligibility criteria below.
Location: CHUM โ Fort-de-France, Martinique
Age range: 18 Years
๐งช Interventions in This Study
- TEST GROUP: A standardised fluid bolus of 8 mL/kg of ideal body weight using Ringer's lactate will be administered in septic shock patients. (OTHER)
- CONTROL GROUP: A standardised fluid bolus of 8 mL/kg of ideal body weight using Ringer's lactate will be administered in non-septic postoperative patients. (OTHER)
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (1 Sites)
- CHUM โ Fort-de-France, Martinique
๐ Contact the Study Coordinator
Phone: (059) 659-2696
Email: SARAH-PRESCILLIA.JOSEPG@CHU6MARTINIQUE.FR
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Sepsis
- A Multicenter Prospective Observational Study to Derive and Verify the Performance of a Host-response Based Diagnostic Tool for Early Detection of Severe Infections. โ New York, New York
- Dynamics of Organ Damage and Immune Exhaustion During Sepsis โ Rochester, Minnesota
- PICS: Subtitle Cardiac Dysfunction in Older Sepsis Survivors โ Gainesville, Florida
- A Validation Study of the Lab Clasp Device: A Point of Care Sepsis Risk Monitor โ Boston, Massachusetts
- A Rapid Diagnostic of Risk in Hospitalized Patients Using Machine Learning โ New Haven, Connecticut
- Sepsis Associated Encephalopathy (SAE) Biomarkers โ Gainesville, Florida
Explore by condition: All Sepsis clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.