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NCT06327633Completed

Effects of Olfactory Training on the Brain Function in T2DM Patients With Mild Cognitive Impairment

A Pilot, Prospective, Randomized, Open Label, Parallel, 4-month Study to Explore and Evaluate the Therapeutic Effects of Olfactory Training on the Cognitive Function, Olfactory Function, and Odor-induced Brain Activation in T2DM Patients With Mild Cognitive Impairment.

Source: ClinicalTrials.gov · Last updated 11 Jul 2025

Brief summary (registry, in English)

This is a prospective, randomized, open label, parallel, 4-month study to explore and evaluate the therapeutic effects of olfactory training on the cognitive function, olfactory function, and odor-induced brain activation in T2DM patients with mild cognitive impairment (MCI).

Status (registry)
Completed
Study type
Interventional
Enrollment
60 (actual)
First submitted
18 Mar 2024
Start date
1 Jan 2024
Primary completion date
15 May 2025
Lead sponsor
The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School
NCT number
NCT06327633

What you commit to

  • Study type: Interventional
  • Participants enrolled: 60
  • From 1 Jan 2024 to the primary completion date, 15 May 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Receive other test drugs currently or within 3 months before participating in the project;
  • Taking cognitive-related drugs.

Other illness

  • Cognitive function assessment suggests normal cognition or dementia;
  • Other dementia related neurological diseases or depression, Mental dysplasia, mania, schizophrenia, etc in the past 2 years; Central nervous system diseases, including brain trauma, intracranial hemorrhage, acute cerebral infarction, etc;
  • Congenital diseases and traumatic history of nose, maxillofacial and skull base affecting olfaction.
  • With symptoms of upper respiratory tract infection, including nasal congestion, runny nose, fever, etc. on the day of MR examination;
  • Severe impairment of heart, liver, kidney and other organs;
  • Known or suspected allergic history to essential oil;

Other

  • Severe sinusitis, nasal cavity and sinus polyps, skull base or nasopharyngeal tumors and other space occupying lesions;
  • Diabetic Acute and chronic complications, including diabetic ketoacidosis, diabetic ketoacidosis; a hyperglycemic hyperosmolar state or severe hypoglycemic coma, etc.
  • Contraindications of MRI examination, such as implantation of metal prosthesis in vivo, claustrophobia, etc;
  • Pregnant and lactating women;

Who the study is looking for

  • patients with type 2 diabetes mellitus;
  • Aged: 40 -75 years ;
  • Cognitive function assessment suggests mild cognitive impairment;
  • A stable glucose-lowering regimen for more than 2 months;
  • ≥6 years of education;
  • Right-handed.

Age in the registry: 40 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Division of Endocrinology, the Affiliated Drum Tower Hospital of Nanjing University
Coordinator of this site? Confirm its status
NanjingChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.