A Clinical Study to Assess the Effect of Tisina Complex on Cognitive Health in Individuals With Mild Cognitive Impairment

Launched by VEDIC LIFESCIENCES PVT. LTD. · Feb 27, 2025

Keywords

ClinConnect Summary

This clinical trial is studying the effects of a treatment called Tisina Complex on cognitive health (how well people think and remember) in individuals who have mild cognitive impairment and also experience tinnitus (a ringing or buzzing in the ears). The study will involve about 112 people aged 30 to 75 years, and it will compare the effects of Tisina Complex to a placebo, which is an inactive substance that looks the same. Participants will be randomly assigned to receive either the active treatment or the placebo for 90 days.

To be eligible for the trial, individuals must be between 30 and 75 years old, agree to participate, and have mild cognitive impairment along with tinnitus that can be measured. Certain health conditions, such as heart disease or severe psychiatric disorders, would exclude someone from participating. Those who join the study can expect to undergo evaluations and assessments throughout the 90 days, with the goal of understanding how Tisina Complex affects their cognitive health. It's important to note that the study is not yet recruiting participants, so those interested will need to wait for it to begin.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • 1. Males and females between 30 - 75 years old (both values included).
• • 2. Individuals willing to provide a signed and dated informed consent and authorization to use personal health information in accordance with local and national guidance and regulations
• • 3. Individuals with mild cognitive impairment as indicated 61 - 82 (both values included).
• • 4. Individuals with subjective tinnitus with normal hearing or up to moderate sensorineural hearing loss for more duration.
• • 5. Tinnitus maskable with noise of at least 5 decibels assessed by audiometry.
• • 6. Individuals with a THI score between 18 to 56 (both values included).
• • 7. Progressive cognitive complaints like stress, disturbed sleep etc. reported by participant or caregiver.
• • 8. Individuals willing to comply with all procedures as outlined in the informed consent.
• Exclusion Criteria:
• • 1. Individuals with a medical history of heart disease, respiratory disorders, seizure disorders, metabolic syndrome or other chronic health conditions requiring medication.
• • 2. Clinically diagnosed with Attention-Deficit/Hyperactivity Disorder (ADHD)
• • 3. Clinical disgnosed with Alzheimer disease
• • 4. Individuals with clinically significant psychiatric or neurological states, neurodegenraitve disorders such as Parkinson's disease \& front-temporal dementia etc that may account for cognitive impairment.
• • 5. Individuals of objective (pulsatile) tinnitus.
• • 6. Individuals with unilateral tinnitus.
• • 7. Individuals suffering with any congenital anomalies which may lead to any otological problem.
• • 8. Individuals suffering from any infective otological problem.
• • 9. Individuals suffering from any otological problem other than tinnitus and sensorineural hearing.
• • 10. Individuals whose tinnitus resulted from acute acoustic trauma, sudden deafness or traumatic head or neck injury.
• • 11. Individuals taking any ototoxic or potentially tinnitus-inducing medication (e.g., aminoglycosides, chemotherapeutics, loop diuretics, high doses of aspirin or quinine).
• • 12. Individual with Maniere's disease, otosclerosis and acute or chronic otitis media.
• • 13. Individuals with history and/or presence significant gastrointestinal disease, active malignant diseases, autoimmune diseases, hemorrhagic diathesis, cardiovascular, renal or hepatic disorders, psychiatric disorders, thyroid disease or any other acute or chronic disease.
• • 14. Individuals who are not willing to maintain their medication, diet or physical activity habits during the study.
• • 15. Individuals with uncontrolled Hypertension with systolic blood pressure more than or equal to 140 and/or diastolic blood pressure more than or equal to 90 mm Hg.
• • 16. Individuals with FBG more than or equal to 126 mg/dl.
• • 17. Aspartate aminotransferase (AST), Alanine aminotransferase (ALT) values exceeding 2 times the upper normal limit.
• • 18. Serum creatinine levels exceeding 1.5 times the upper normal limit.
• • 19. Head injury immediately preceding cognitive deterioration.
• • 20. History of uncontrolled migraine headaches, severe sleep disorders.
• • 21. Use of psychotropic drugs or any other drug or supplement such as nootropics that may significantly affect cognitive functioning during the month prior to psychometric testing.
• • 22. Use of any experimental medication or OTC medication or herbal treatment such as hesperidin, diosmin and other flavonoids within 1 month prior to screening.
• • 23. Females taking any oral contraceptives.
• • 24. Current smokers.
• • 25. Consumption of excessive amount of caffeine i.e.≥ 4 cups daily (\> 500 mg per day).
• • 26. History of drug, substance or alcohol addiction or abuse within the past 12 months.
• • 27. Prior participation in a clinical study in the past 90 days before screening.
• • 28. Females who are pregnant/planning to be pregnant or currently lactating.