Skip to content

Efficacy of inflawell capsules on behavioral and cognitive symptoms and DTI changes in patients with frontotemporal dementia

Efficacy of inflawell capsules containing Boswellic acids on behavioral and cognitive symptoms and DTI changes in patients with frontotemporal dementia

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170315033086N8
Enrollment
20
Registered
2021-01-06
Start date
2019-09-23
Completion date
Unknown
Last updated
2021-02-22

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

Conditions

Frontotemporal dementia. Frontotemporal dementia

Interventions

Intervention group: inflawell receiving group, 3 month, 3 times/day, oral administration (400 mg), inflawell containing Boswellic acids powders was manufactured in KondorPharma pharmaceutical Company

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Behavioral variant of Frontotemporal dementia based on guideline: Rascovsky K, Hodges JR, Knopman D, et al. Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia. Brain. 2011;134 Language variant of Frontotemporal dementia based on guideline: Gorno-Tempini ML, Hillis AE, Weintraub S, et al. Classification of primary progressive aphasia and its variants. Neurology. 2011;76:1006-1014

Exclusion criteria

Exclusion criteria: Other specific diseases of the central nervous system such as Parkinson's, multifactorial dementia, anterior brain dementia, Huntington's disease, hydrocephalus, brain tumors confirmed by MRI, severe paralysis of the nerve of the supernuclear body, epilepsy, clots between layers of brain tissue, multiple sclerosis and other dementias Taking NSAIDs and systemic corticosteroids for previous two months continuously Severe cardiovascular disease, kidney and liver disorders Psychiatric disorders include bipolar disorder and schizophrenia under medication Drugs or alcohol abuse Brain-related surgical interventions head trauma and progressive degenerative motor disorder Metabolic and systemic diseases

Design outcomes

Primary

MeasureTime frame
Changes in the lesion area of brain. Timepoint: At the commencement of the investigation and 3 months after taking inflawell. Method of measurement: MRI ( Diffusion Tensor Imaging).

Secondary

MeasureTime frame
Changes in cognitive and behavioral symptoms. Timepoint: At the commencement of the investigation and 3 months after taking inflawell. Method of measurement: Clinical cognitive tests: Behavioral inventory and FTD-Clinical dementia rating (FTD-CDR), Neuropsychiatry inventory (NPI), Frontal assessment buttery (FAB), Persian naming test (PNT).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactVajihe Aghamolie

Tehran University of Medical Sciences

vajiheh102@gmail.com+98 21 5541 9151

Outcome results

None listed

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