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Molar Sodium Lactate Filling in Severe Meningeal Hemorrhage

Effect of Molar Sodium Lactate Filling on Cerebral Hemodynamics in Patients With Severe Meningeal Hemorrhage Multicenter Randomized Study

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04141371
Enrollment
3
Registered
2019-10-28
Start date
2022-02-14
Completion date
2024-06-07
Last updated
2025-03-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Subarachnoid Hemorrhage, Aneurysmal

Brief summary

Subarachnoid hemorrhage by aneurysmal rupture is a serious condition associated with a high mortality rate. Among the complications presented by these patients, vasospasm is one of the main causes of secondary aggravation, in particular the appearance of delayed neurological deficits following the induced cerebral ischemia. Classically occurring between the 4th and 12th day, with a peak on D7, its prevention is currently often ineffective. In recent years, many studies have shown that sodium lactate could be an interesting product for neuroprotection. In addition to an anti-osmotic effect that has been demonstrated by our team in the context of post-traumatic intracranial hypertension, a metabolic action has also been observed in periods of metabolic attacks induced by brain attacks. Recently, a vasodilatory action of sodium lactate has been observed from an experimental and clinical point of view. The purpose of this work is to observe the effect of sodium lactate, compared to placebo, on cerebral hemodynamics measured by perfusion CT (Mean Transit Time MTT) in a population of patients with hemorrhage under the arachnoid. This work is the preliminary work of a study that will investigate the potential preventive protective effect of sodium lactate on the incidence of vasospasm.

Interventions

daily saline infusion over 3 hours during the vasospasm period

DRUGMolar Sodium Lactate

daily 3-hour infusion of sodium molar lactate during the vasospasm period

Sponsors

Centre Hospitalier Universitaire de Nice
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Masking description

paticipant and radiologists are masked

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Any patient over 18 years of age with severe meningeal hemorrhage defined by a WFNS≥3 score will be included in the study. * Treated by endovascular embolization or surgically within 48 hours * After obtaining the informed consent of the patient, or his relatives if he is not searchable (coma). * Affiliation to a social security system * After an adapted preliminary medical examination

Exclusion criteria

* Post-traumatic meningeal hemorrhage * Management time \>48h with respect to bleeding * Known neurodegenerative pathology (Alzheimer's, Parkinson's, etc.), Creutzfeldt-Jacob disease * Pregnant woman * Decision not to treat * Refusal to participate in the study * Adult patient protected by law * Person deprived of administrative or judicial freedom

Design outcomes

Primary

MeasureTime frameDescription
median transit time (MTT)7 daysmedian transit time (MTT) in seconds, on the perfusion scanner on 6 regions of the brain between D0 and D7 of the product perfusion

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026