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Case-control Study on the Phenomenon and Regularity of Acupoint Hyperalgesia in Non-small Cell Lung Cancer

Case-control Study on the Phenomenon and Regularity of Acupoint Hyperalgesia in Non-small Cell Lung Cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400086487
Enrollment
Unknown
Registered
2024-07-02
Start date
2024-07-02
Completion date
Unknown
Last updated
2024-07-08

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

Non-small Cell Lung Cancer group:No intervention
Healthy control group:No intervention

Sponsors

The Third Affiliated Hospital of Zhejiang Chinese Medical University (Zhongshan Hospital of Zhejiang Province)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: ? 18 years old = age = 80 years old, gender is not limited; ? Those who meet the relevant cancer diagnostic criteria and whose diagnosis is confirmed by pathological tissue examination; ? Carpenter's score =50; ? Willing to cooperate with the study and sign the informed consent form;

Exclusion criteria

Exclusion criteria: ? Combined serious primary diseases of respiratory, circulatory, urinary, haematological and nervous systems; ? Those who have indwelling needles in the limbs of the detection point area; ? Those who have skin breakage or suffer from skin disease in the testing point area; ? After cancer pain nerve block surgery; ? Those who have insufficient cognitive ability to complete the questionnaire independently; ? Those who have insufficient cognitive ability to complete the questionnaire independently; ? Those with BMI = 25 points;

Design outcomes

Primary

MeasureTime frame
pressure-pain threshold;Rate of acupoint hyperalgesia;

Secondary

MeasureTime frame
General information;

Countries

CHINA

Contacts

Public ContactYi Liang

Zhejiang Chinese Medical University

34722092@qq.com+86 180 5710 2850

Outcome results

None listed

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