Skip to content

Evaluation of therapeutic effects of bacopa monnieri on neuropsychologic profile resulting from traumatic brain injury

Evaluation of therapeutic effects of bacopa monnieri on neuropsychologic profile resulting from traumatic brain injury: a randomized, double-blind, placebo-controlled trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240813062745N1
Enrollment
100
Registered
2024-10-02
Start date
2024-09-22
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

Injuries to the head. Injuries to the head

Interventions

Intervention 1: Two 160 mg capsules of the standardized drug Bacopa from Darukodeh with the brand name Memocopa and a capsule similar to the original drug made in the pharmaceutical laboratory of Yazd

Sponsors

Yazd University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Sign the written consent Patients with known traumatic brain injury according to the opinion of the attending physician Incidence of dementia caused by traumatic brain injury based on Eden Brook index score Age 18 to 65 years Not suffering from dementia or Alzheimer's disease before brain trauma A minimum of two weeks and a maximum of one year have passed since the occurrence of brain trauma.

Exclusion criteria

Exclusion criteria: Taking antidepressants including SSRI, SNRI, TCA, MOAI8. The presence of pregnancy, breastfeeding Previous history of dementia Suffering from hypothyroidism Kidney problems Liver problems The presence of heart disease / bradycardia / arrhythmia Suffering from serious metabolic disease Suffering from severe depression Contradiction of Bacopa drug History of covid affecting memory Taking drugs that may cause cognitive impairment, such as topiramate, anticholinergics

Design outcomes

Primary

MeasureTime frame
Neuropsychological profile. Timepoint: Before the start of the intervention, one month after the start of the intervention and three months after the start of the intervention. Method of measurement: 1- Addenbrooke's Cognitive Test Revised Version (ACE-R) 2- Benton's Acceptance Test 3- Depression, Anxiety, Stress Scale (DASS-21) 4- Rancho Los Amigos Cognitive Function Scale (RLAS) 5- Glasgow coma scale 6- John Ridley Stroop test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactReza Bidaki

Yazd University of Medical Sciences

reza_bidaki@yahoo.com+98 912 195 5521

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026