# Validation of a Capillary Leak Index During Septic Shock, Based on Haemoglobin Level Variations Induced by Fluid Resuscitation. A Pilot Study.

> **NCT07733206** · NA · NOT_YET_RECRUITING · sponsor: **University Hospital Center of Martinique** · enrollment: 100 (estimated)

## Conditions studied

- Sepsis

## Interventions

- **OTHER:** 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.

## Key facts

- **NCT ID:** NCT07733206
- **Lead sponsor:** University Hospital Center of Martinique
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** NOT_YET_RECRUITING
- **Start date:** 2026-09-15
- **Primary completion:** 2028-10-15
- **Final completion:** 2028-10-15
- **Target enrollment:** 100 (ESTIMATED)
- **Last updated:** 2026-07-29


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT07733206

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT07733206, "Validation of a Capillary Leak Index During Septic Shock, Based on Haemoglobin Level Variations Induced by Fluid Resuscitation. A Pilot Study.". Retrieved via MORVS 2026-10-20 from https://api.morvs.ai/clinical/NCT07733206. Licensed CC0.

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