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A case-control study on the phenomenon of pain sensitisation at acupoints and its pattern in patients with different types of cancer

A case-control study on the phenomenon of pain sensitisation at acupoints and its pattern in patients with different types of cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500095711
Enrollment
Unknown
Registered
2025-01-10
Start date
2025-01-15
Completion date
Unknown
Last updated
2025-05-19

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

Conditions

Lung cancer, colorectal cancer

Interventions

Healthy control group:NA
Colorectal cancer grou:NA

Sponsors

The Third Affiliated Hospital of Zhejiang Chinese Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Cancerous person 1. 18 years old =50; 4.Willing to cooperate with the study and sign the informed consent form; Note: Participants must meet all of the above four criteria. Healthy participants: 1. Aged 18 to 80 years, inclusive, without gender restrictions; 2. Have not been diagnosed with any significant illness within the past year; 3. Possess no history of anxiety or depression; 4. Demonstrate a willingness to collaborate in clinical research and are capable of providing informed consent. Note: Participants must meet all of the above four criteria.

Exclusion criteria

Exclusion criteria: Cancerous person 1.Severe primary disease with respiratory, circulatory, urinary, blood, nervous and other systems; 2.Detect limb disorders, skin damage and nerve sensation abnormalities in the acupoint area; 3. BMI>=28 points; 4.The cognitive ability of questionnaire survey is insufficient, can not complete the questionnaire independently Note: Any individual meeting any one of the above criteria will be excluded. Healthy participants: 1. Women who are menstruating, breastfeeding, or pregnant; 2. Individuals with skin damage in the area to be tested. Note: Any individual meeting any one of the above criteria will be excluded.

Design outcomes

Primary

MeasureTime frame
Pressure-pain threshold;

Countries

China

Contacts

Public ContactNie Na

The Third Affiliated Hospital of Zhejiang Chinese Medical University

niena0616@126.com+86 178 1612 5750

Outcome results

None listed

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