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Screening and diagnostics of Alzheimer's disease based on exhaled breath analysis

Screening and diagnostics of Alzheimer's disease based on exhaled breath analysis

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300075674
Enrollment
Unknown
Registered
2023-09-12
Start date
2023-09-01
Completion date
Unknown
Last updated
2023-09-18

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

Conditions

Alzheimer’s disease

Interventions

non-AD cognitive impairment group:NA
Cognitively unimpaired healthy control group:NA

Sponsors

Tianjin Medical University General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 85 Years

Inclusion criteria

Inclusion criteria: (1) Cohort 1 (AD group. n=150) 1) Age greater than 50 and less than 85 years old; 2) Diagnosed with AD according to IWG-2 criteria; 3) Did not receive disease-modifying therapy before exhaled breath sample collection; 4) Patients have been fully informed, agreed to participate in the program, and are expected to complete the examination related to the program. (2) Cohort 2 (non-AD cognitive impairment group, n=150) 1) Age greater than 50 and less than 85 years old; 2) Cognitive impairment due to other neurological diseases, including vascular cognitive impairment, frontotemporal lobar degeneration, and dementia with Lewy bodies; 3) Patients have been fully informed, agreed to participate in the program, and are expected to complete the examination related to the program. (3) Cohort 3 (Cognitively unimpaired healthy control group, n=150) 1) Age greater than 50 and less than 85 years old; 2) Having no subjective cognitive decline complaints and normal performance in objective neuropsychological tests

Exclusion criteria

Exclusion criteria: 1) Need respiratory support (oxygen, non-invasive ventilator, etc.); 2) Unable to obtain sufficient expired air due to respiratory restriction 3) Breastfeeding or pregnant women; 4) Poor compliance, unwillingness to accept the examination, or unwillingness to complete the follow-up.

Design outcomes

Primary

MeasureTime frame
The primary outcome will be the mass-to-charge ratios of volatile organic compounds (VOCs) in exhaled breath from subjects.;

Countries

China

Contacts

Public ContactNan Zhang

Tianjin Medical University General Hospital

nkzhangnan@163.com+86 22 6036 2255

Outcome results

None listed

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