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Clinical study on accelerated aging of the tumor system

Clinical study on accelerated aging of the tumor system

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500096969
Enrollment
Unknown
Registered
2025-02-10
Start date
2025-01-16
Completion date
Unknown
Last updated
2025-02-17

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

Conditions

Non-small cell lung cancer

Interventions

Case group:None
Control group:None

Sponsors

Quzhou People Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Healthy people Inclusion Criteria: 1.15 6.5% or fasting blood glucose >126 mg/dL or taking diabetes medication or insulin therapy); j. Recent cardiovascular disease events (myocardial infarction, coronary intervention, coronary artery bypass grafting); k. Infectious diseases such as HIV, hepatitis, tuberculosis, etc.; l. Hand or lower limb disability that interferes with normal function and life. 4. Able to communicate well with the investigator and be able to cooperate with various tasks during the research period. 5. Written informed consent can be signed voluntarily. Patients with non-small cell lung cancer Inclusion Criteria: 1. Age 40-60 years old, 15 = BMI= 28, male or female. 2. Local residents of Quzhou or have lived in Quzhou for the past 10 years and have no major bad habits. 3. No other malignant tumors or history of tumors except non-small cell lung cancer. 4. Tumor does not have orthotopic and distant metastases (mainly stage IA-II). 5. Have not used any chemotherapy drugs within 2 years prior to enrollment. 6. Able to communicate well with the investigator and be able to cooperate with various tasks during the research period. 7. Written informed consent can be signed voluntarily.

Exclusion criteria

Exclusion criteria: Healthy people Exclusion Criteria: 1. Women who are pregnant, lactating or suffering from premature ovarian failure, hysterectomy/endometrial dissection. 2. Currently taking the following medications: a. Chemotherapy drugs (e.g. tamoxifen, doxorubicin, etc.); b. Antiplatelet agents (e.g., clopidogrel/plavix, dipyridine/anglenol, ticlopidine/ticlopidine, except aspirin); c. Cholinesterase inhibitors (e.g., donepezil/alicept). 3. Treatment with any investigational drug or device within 30 days prior to enrollment, or participation in any other clinical trial within 3 months prior to enrollment, or injection of vaccine within half a month prior to enrollment. Patients with non-small cell lung cancer Exclusion Criteria: 1. Women with premature ovarian failure, hysterectomy/endometrial dissection. 2. Currently taking the following medications: a. Chemotherapy drugs (e.g. tamoxifen, doxorubicin, etc.); b. Antiplatelet agents (e.g., clopidogrel/plavix, dipyridine/anglenol, ticlopidine/ticlopidine, except aspirin); c. Cholinesterase inhibitors (e.g., donepezil/alicept). Treatment with any investigational drug or device within 30 days prior to enrollment, or participation in any other clinical trial within 3 months prior to enrollment, or vaccine injection within half a month prior to enrollment.

Design outcomes

Primary

MeasureTime frame
Serum NAD+ level;

Secondary

MeasureTime frame
Bone density;Grip strength test;FVC;Flexibility of fingers;

Countries

China

Contacts

Public ContactZhang Feng

Quzhou People Hospital

felixfzhang@163.com+86 570 3055178

Outcome results

None listed

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