Cytoflavin in the Rehabilitation of Post-intensive Care Syndrome in Stroke Survivors

Ischemic Stroke Clinical Trial

Official title:

Use of Cytoflavin Solution at the Time of Early Rehabilitation in Patients With Post-intensive Care Syndrome Who Underwent Ischemic Stroke

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04194229
• Other study ID #: PR-C
• Status: Completed
• Start date: November 11, 2016
• Est. completion date: January 2021

Study information

• Verified date: December 2021
• Source: POLYSAN Scientific & Technological Pharmaceutical Company
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Objective - to assess the effect of Cytoflavin® and its tolerability within the integrated program of rehabilitation of patients who underwent ischemic stroke

Description:

Cerebral stroke (CS) remains one of the key issues of modern society, being a predominant cause of deep and persistent disability of the population. Huge social and economic damage arising from cerebrovascular diseases raises the problem of improving medical care for strokes among the most relevant scientific and practical tasks of neurology Regulation of energy metabolism is considered a powerful tool for acute conditions relief, including those that occur due to acute impairment of cerebral blood flow. A number of adjuvant energy protector concomitant medications with systemic pharmacodynamic properties based on signaling (hormonal) and substrate mode of action of succinic acid and other mitochondrial substrates and co-factors was created for this A significant role in the rehabilitation of patients who underwent CS is assigned to the treatment of complications of care in the intensive care unit, the so-called post-intensive care syndrome (PICS), which is a set of somatic, neurological, social and psychological consequences of periods in intensive care unit (ICU) conditions that bring limitations to the patient's daily activities In the Brain Institute Clinic (Ekaterinburg), the first results of the metabolic status monitoring during physical and cognitive exercise in patients with PICS were obtained. These results prove that control over metabolic state holds the promise of developing approaches to increasing exercise tolerance Taking into account the effectiveness of Cytoflavin® in treatment of acute impairment of cerebral circulation and consequences of cerebrovascular diseases, on the one hand, and its classification as a metabotropic energy corrector, on the other hand, the evaluation of Cytoflavin® medication tolerability in the integrated program of neurorehabilitation of patients with PICS after ischemic stroke presents a significant interest.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 60
• Est. completion date: January 2021
• Est. primary completion date: January 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Men and women aged 18 years and above;
• Patients who underwent ischemic stroke;
• The period from the development of ischemic stroke is not less than 12 and not more than 28 days;
• Staying in intensive care unit for no less than 72 hours;
• Diagnosed post-intensive care syndrome (PICS);
• Functional status assessed using the modified Rankin scale amounts to 4-5;
• Gravity gradient of 20° to 40° upon inclusion in observational non-interventional program

Exclusion Criteria:

• Vegetative state;
• Mechanical ventilation lasting more than 72 hours after the development of ischemic stroke;
• Surgical treatment for cerebral stroke (decompressive craniectomy; thromboextraction etc.);
• Premorbid (before the development of ischemic stroke) level of functional activity assessed using the modified Rankin scale amounts to 4 or 5;
• Signs of increasing neurological deficit or enlargement of hypoperfusion zones on CT scans within 24 hours before inclusion in observational non-interventional program;
• Level of consciousness = 5 according to Glasgow Coma Scale and/or = 1 according to Richmond Agitation-Sedation Scale (RASS);
• Behavioral Pain Scale (BPS) or Visual Analogue Scale assessment score of more than > 0 at the moment of inclusion;
• Systolic blood pressure < 90 and > 180 mm Hg;
• Diastolic blood pressure = 110 mm Hg;
• Mean ABP < 60 mm Hg;
• Clinical and/or electrocardiographic signs of acute coronary syndrome (including de novo ST elevation or depression, negative T-waves amplitude formation and buildup, formation of pathological Q-wave, increase in the level of markers of myocardial injury - troponin T or I, creatine phosphokinase-MB, LDH-1), or diagnosed acute myocardial infarction occurring within a month before inclusion in observational program;
• Acute heart arrhythmias;
• Heart rate (HR) < 60 or > 100 per minute;
• Spontaneous respiration rate (RR) < 10 or > 30 per minute;
• Arterial oxygen saturation (SpO2) < 90 %;
• Venous serum glucose level = 4 mmol/L;
• Axillary body temperature = 38.5 °C;
• Hematocrit = 30 %;
• Level of hemoglobin = 80 g/l;
• Serum total protein = 55 g/l;
• Positive passive leg raising test (PRL-test);
• Acute heart failure;
• Acute respiratory failure;
• Acute kidney injury;
• Acute liver cell failure;
• Congestive heart failure;
• Chronic respiratory failure, stage greater than I;
• Chronic kidney disease with estimated glomerular filtration rate using Cockcroft-Gault formula < 60 ml/min/1.73 m2;
• Clinically significant deviations in the results of complete blood count, blood chemistry, common urine analysis, except those that are acceptable according to other non inclusion criteria;
• Purulent-inflammatory diseases at any location;
• Refuse of the patient to undergo verticalization or exercise sessions;
• Use of medicinal products belonging to the pharmaceutical therapeutic category of metabolic drugs at the time of inclusion in observational non-interventional program, as well as plans for their use during study;
• Plans for use of physical rehabilitation methods other than verticalization and cycling exercise sessions during the course of the program.

Related Conditions & MeSH terms

• Ischemia
• Ischemic Stroke
• Post Intensive Care Unit Syndrome
• Stroke
• Syndrome

Locations

Country	Name	City	State
Russian Federation	Brain Institute Clinic	Ekaterinburg	Sverdlovsk Region

Sponsors (1)

Lead Sponsor	Collaborator
POLYSAN Scientific & Technological Pharmaceutical Company

Country where clinical trial is conducted

Russian Federation, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Median time to achieving gravity gradient of 90°	Median time (in days) to achieving gravity gradient of 90°.	10 days
Secondary	Proportion of patients who achieved gravity gradient of 90°	Proportion of patients who achieved gravity gradient of 90° by day 5 and 10 days of rehabilitation activities	5 and 10 days
Secondary	Change in of oxygen consumption during 90° verticalization	Change in of oxygen consumption during 90° verticalization	5 and 10 days
Secondary	Change in the Medical Research Council (MRC) scale for muscle strength score	Medical Research Council scale for muscle power (MRC), where 0 - tetraplegia, 60 - normal value	5 and 10 days
Secondary	Change in Barthel index (BI)	Barthel index (BI), when 0 - complete inability to self-service, 100 - full capability of self-service	5 and 10 days of rehabilitation activities
Secondary	Change in Modified Rankin scale (MRS) score	Modified Rankin scale (MRS), when 0 - no disability, 5 - severe disability	5 and 10 days of rehabilitation activities