# A Single Centre Study Comparing Continuous Interstitial Fluid Lactate Detection to Standard Measurements of Lactate in Patients Undergoing Elective Coronary Artery Bypass Graft Surgery and/or Valve Replacement.

> **NCT06602336** · NA · RECRUITING · sponsor: **Queen Mary University of London** · enrollment: 50 (estimated)

## Conditions studied

- Coronary Artery Bypass
- Coronary Artery Bypass Graft
- Coronary Artery Bypass Graft Surgery (CABG)
- Valve Replacement
- Valve Surgery
- Cardiovascular
- CABG

## Interventions

- **DEVICE:** Continuous Lactate Monitoring Device

## Key facts

- **NCT ID:** NCT06602336
- **Lead sponsor:** Queen Mary University of London
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** RECRUITING
- **Start date:** 2025-05-20
- **Primary completion:** 2026-05-01
- **Final completion:** 2026-05-01
- **Target enrollment:** 50 (ESTIMATED)
- **Last updated:** 2026-01-07


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT06602336

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT06602336, "A Single Centre Study Comparing Continuous Interstitial Fluid Lactate Detection to Standard Measurements of Lactate in Patients Undergoing Elective Coronary Artery Bypass Graft Surgery and/or Valve Replacement.". Retrieved via AI Analytics 2026-06-09 from https://api.ai-analytics.org/clinical/NCT06602336. Licensed CC0.

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