A Lithium-Based Medication to Improve Neurological Outcomes After Surgical Carotid Reconstruction

Sponsor
Negovsky Reanimatology Research Institute (Other)
Overall Status
Recruiting
CT.gov ID
NCT05126238
Collaborator
Demikhov Municipal Clinical Hospital 68 (Other)
500
1
2
36
13.9

Study Details

Study Description

Brief Summary

There are 10.3 million cases of stroke registered in the world every year; 63% of them lead to death. According to World Health Organization, stroke is one of the most important risk factors of death and early disability.

Carotid artery surgery is a gold standard of hemodynamically significant carotid artery disease treatment. According to some trials, carotid artery surgery decreases the 2-years mortality.

The most important part of carotid artery surgery is a temporary absence of blood flow in the carotid artery. The duration of this period is a crucial characteristic of this type of surgery. The absence of blood flow leads to brain ischemia which is the risk factor of postoperative neurocognitive disorders such as emergence delirium, postoperative delirium and postoperative cognitive dysfunction.

Some surgical and non-surgical methods for brain protection were evaluated. According to recent data, there is no evidence of effective pharmacological protective methods that can decrease brain damage during carotid artery surgery.

Nevertheless, some trials demonstrated that using lithium-based medications for patients with a stroke can reduce the volume of the stroke. Therefore, the investigators want to check the hypothesis that using lithium-based medication in the preoperative period can reduce brain damage during carotid artery surgery.

The objectives of this trial:
  1. To determine if Lithium carbonate is superior to placebo for the occurrence of emergence delirium, agitation, postoperative delirium and postoperative cognitive dysfunction.

  2. To determine if Lithium carbonate is non-inferior to placebo for the occurrence of a new arrhythmia, leukocytosis, acute kidney injury, seizure disorders, diarrhea, nausea, and vomit.

Condition or Disease Intervention/Treatment Phase
  • Drug: Lithium Carbonate
  • Drug: Placebo
Phase 3

Detailed Description

There are 10.3 million cases of stroke registered in the world every year; 63% of them lead to death. According to World Health Organization, stroke is one of the most important risk factors of death and early disability.

Carotid artery surgery is a gold standard of hemodynamically significant carotid artery disease treatment. According to some trials, carotid artery surgery decreases the 2-years mortality.

The most important part of carotid artery surgery is a temporary absence of blood flow in the carotid artery. The duration of this period is a crucial characteristic of this type of surgery. The absence of blood flow leads to brain ischemia which is the risk factor of postoperative neurocognitive disorders such as emergence delirium, postoperative delirium and postoperative cognitive dysfunction.

Some surgical and non-surgical methods for brain protection were evaluated. According to recent data, there is no evidence of effective pharmacological protective methods that can decrease brain damage during carotid artery surgery.

Nevertheless, some trials demonstrated that using lithium-based medications for patients with a stroke can reduce the volume of the stroke. Therefore, the investigators want to check the hypothesis that using lithium-based medication in the preoperative period can reduce brain damage during carotid artery surgery.

The objectives of this trial:

To determine if Lithium carbonate is superior to placebo for the occurrence of emergence delirium, agitation, postoperative delirium and postoperative cognitive dysfunction.

To determine if Lithium carbonate is non-inferior to placebo for the occurrence of a new arrhythmia, leukocytosis, acute kidney injury, seizure disorders, diarrhea, nausea, and vomit.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
500 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
A Lithium-Based Medication to Improve Neurological Outcomes After Surgical Carotid Reconstruction: A Double-Blind, Placebo Control Randomized Trial (BINOS)
Actual Study Start Date :
Nov 20, 2021
Anticipated Primary Completion Date :
Dec 20, 2023
Anticipated Study Completion Date :
Nov 20, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Lithium

In preoperative period patients will take 300mg of lithium carbonate on 1-1-1 regimen during 2 days prior to surgery. On the day of surgery, they will take 300mg of lithium carbonate 2 hours before surgery. After the surgery, patients will take 300mg of lithium carbonate in the afternoon and 300mg of lithium carbonate in the evening.

Drug: Lithium Carbonate
In preoperative period patients will take 300 mg of lithium carbonate on 1-1-1 regimen during 2 days prior to surgery. On the day of surgery they will take 300mg of lithium carbonate 2 hours before surgery.

Placebo Comparator: Placebo

In preoperative period patients will take placebo on 1-1-1 regimen during 2 days prior to surgery. On the day of surgery, they will take placebo 2 hours before surgery. After the surgery, patients will take placebo in the afternoon and in the evening.

Drug: Placebo
In preoperative period patients will take placebo on 1-1-1 regimen during 2 days prior to surgery. On the day of surgery they will placebo 2 hours before surgery.

Outcome Measures

Primary Outcome Measures

  1. Frequency of emergence delirium [30 days]

    Number of patients with positive the confusion assessment method for the intensive care unit as soon as they reach Aldrete score of 9 points

Secondary Outcome Measures

  1. Frequency of agitation [30 days]

    Richmond agitation-sedation scale more or equal +2 evaluated from the end of volatile anesthetic supply to the moment when a patient reaches Aldrete score of 9 points Richmond agitation-sedation scale: minimum value = -5 (Unarousable - no response to voice or physical stimulation) maximum value = +4 (Combative - overtly combative or violent; immediate danger to staff) Adequate patients have the results of Richmond agitation-sedation score equal 0 (Alert and calm; Spontaneously pays attention to caregiver)

  2. Frequency of postoperative delirium [30 days]

    Number of patients with even one positive confusion assessment method for the intensive care unit or 3-minute confusion assessment method

  3. Length of postoperative delirium [until 1 month after surgery]

    30 days - number of days in which patient had positive confusion assessment method for the intensive care unit or 3-minute confusion assessment method

  4. Frequency of overt strokes [1 year]

    Number of overt strokes

  5. Frequency of covert strokes [1 year]

    Number of covert strokes

  6. Length of stay in intensive care unit [1 month]

    Number of days in intensive care unit

  7. Length of hospitalization [1 month]

    Number of days in hospital

  8. Frequency of cardiac death [1 year]

    Number of of cardiac deaths

  9. Frequency of non-fatal cardiac arrest [1 year]

    Number of non-fatal cardiac arrests

  10. Frequency of major adverse cardiac event [1 year]

    Number of major adverse cardiac events

  11. Frequency of major adverse cardiac and cognitive event [1 year]

    Number of major adverse cardiac and cognitive events

  12. 30-days mortality [30 days]

    Number of deaths in period of 30 days after surgery

  13. 1-year mortality [1 year]

    Number of deaths in period of 1 year after surgery

  14. Frequency of new postoperative arrhythmia [1 month]

    Number of new postoperative arrhythmias

  15. Frequency of leukocytosis [From 2 days before surgery to the day of surgery]

    Number of patients with leukocytosis

  16. Frequency of acute diarrhea [From 2 days before surgery to the day of surgery]

    Number of patients with acute diarrhea

  17. Frequency of postoperative nausea and vomit [1 month]

    Number of patients with postoperative nausea and vomit

  18. Frequency of preoperative nausea and vomit [From 2 days before surgery to the day of surgery]

    Number of patients with preoperative nausea and vomit

  19. Frequency of acute kidney injury [1 month]

    Number of patients with acute kidney injury

  20. Frequency of myasthenia [From 2 days before surgery to the day of surgery]

    Number of patients with myasthenia

  21. Frequency of preoperative seizure [From 2 days before surgery to the day of surgery]

    Number of patients with seizure

  22. Frequency of postoperative seizure [1 month]

    Number of patients with seizure

  23. Serum level of S100 beta protein [2 days after surgery]

    Serum level of S100 beta protein

  24. Serum level of neuron-specific enolase [2 days after surgery]

    Serum level of neuron-specific enolase

  25. Serum level of Tau-protein [2 days after surgery]

    Serum level of Tau-protein

  26. Serum level of Neurofilament light polypeptide [2 days after surgery]

    Serum level of Neurofilament light polypeptide

  27. Serum level of Glial fibrillary acidic protein [2 days after surgery]

    Serum level of Glial fibrillary acidic protein

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • age > 18 years

  • elective carotid artery surgery

  • general anesthesia

  • written informed consent

Exclusion Criteria:
  • urgent surgery

  • recent ( < 1 month) overt stroke

  • Mini-mental State Examination < 20 points

  • The presence of any mental disorder according to the International Classification of Diseases 11th Revision which is confirmed by a psychiatrist.

  • The presence of any neuromuscular disease according to the International Classification of Diseases 11th Revision

  • Hypersensitivity or known allergy to lithium carbonate

  • History of seizure disorder

  • History of leukemia

  • Estimated glomerular filtration rate < 30 ml/min/1.73 m2

  • Left ventricular ejection fraction < 30%

  • Heart failure equal 3 or 4 class according to the New York Heart Association Functional Classification

  • Pregnant or breast-feeding women

  • Inability to undergo a preoperative assessment for any reason

  • Previously enrolled in this trial

Contacts and Locations

Locations

Site City State Country Postal Code
1 Demikhov Municipal Clinical Hospital 68 Moscow Russian Federation

Sponsors and Collaborators

  • Negovsky Reanimatology Research Institute
  • Demikhov Municipal Clinical Hospital 68

Investigators

  • Principal Investigator: Valery Likhvantsev, PhD, Negovsky Reanimatology Research Institute

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Valery Likhvantsev, MD, Head of the Research V. Negovsky Reanimatology Research Institute, Negovsky Reanimatology Research Institute
ClinicalTrials.gov Identifier:
NCT05126238
Other Study ID Numbers:
  • BINOS
First Posted:
Nov 18, 2021
Last Update Posted:
Mar 18, 2022
Last Verified:
Mar 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Valery Likhvantsev, MD, Head of the Research V. Negovsky Reanimatology Research Institute, Negovsky Reanimatology Research Institute
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 18, 2022