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Phenolic Complex k110-42 Therapy on Cognitive Functions in Down Children

M

Mansoura University

Status and phase

Not yet enrolling
Phase 3

Conditions

Cognitive Functions

Treatments

Drug: Neumentix
Drug: Phenolic complex k110-42

Study type

Interventional

Funder types

Other

Identifiers

NCT07284693
Ms.25.04.3157

Details and patient eligibility

About

The goal of this study is to evaluate the efficacy of phenolic complex k110-42 on cognitive function of children with Down syndrome

Full description

Children with Down syndrome (DS) often face a variety of cognitive and developmental challenges. These challenges may include delays in speech, motor skills, and social-emotional development. Among these, difficulties with attention and focus are particularly prominent, making it harder for children with DS to participate in academic and everyday activities.

One promising avenue for improving cognitive function is the use of natural compounds with neuroprotective and cognitive-enhancing properties. The phenolic complex K110-42 (Neumentix), derived from the extract of spearmint, has garnered attention for its potential benefits in cognitive performance.

Specifically, polyphenols contained within the aqueous extracts from the Lamiaceae family could mechanistically account for the reported benefits on cognitive performance. Polyphenols found in aqueous extracts of spearmint such as salvianolic and rosmarinic acids have been shown to have anti-oxidant, anti-inflammatory, anti-acetylcholinesterase, and neuroprotective biological activity both in vitro and in vivo .

Phenolic offers a number of benefits on cognitive functions and it is plausible that its anti-inflammatory, antioxidant, anti-fibrotic effects, enhance attention, improving vascular endothelial functions and enhancement of metabolic performances. Because of the multiple functions, phenolic has direct effects on attention deficit in DS.

Enrollment

108 estimated patients

Sex

All

Ages

4 to 8 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Children diagnosed with Down syndrome (Non disjunction Trisomy 21) based on genetic testing .
  • Age between 4-8 years old .
  • Down syndrome children presented with difficulties in attention or focus as reported by parents or based on prior clinical assessments.

Exclusion criteria

  • Parents' refusal.
  • Down syndrome children with other significant developmental or neurological disorders (e.g., autism spectrum disorder, epilepsy).
  • Patients with any chronic illness as liver or renal dysfunction; inflammatory diseases; autoimmune disease; cancer, acute cardiovascular event, eating disorders (anorexia, bulimia) or gastrointestinal disorders.
  • Presence of hypersensitivity to spearmint or any components of Neumentix (Neumentix may increase kidney or liver damage if used in large amounts).
  • Use of stimulant ADHD medication or cognitive-enhancing supplements .
  • IQ test less than 55%.
  • Patients with hypothyroidism.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

108 participants in 2 patient groups, including a placebo group

Phenolic complex k110-42
Active Comparator group
Description:
900mg/kg oral once sachet for 6 month
Treatment:
Drug: Phenolic complex k110-42
Neumentix
Placebo Comparator group
Description:
Sachet once for 6 month
Treatment:
Drug: Neumentix

Trial contacts and locations

0

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Central trial contact

Haidi Sameh Elassal, Master

Data sourced from clinicaltrials.gov

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