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Clinical study of the phenomenon and regularity of acupoint sensitization of colorectal cancer

Not Applicable
Recruiting
Conditions
Colorectal cancer
Registration Number
ITMCTR2000003374
Lead Sponsor
Chengdu University of Traditional Chinese Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

(1) Aged 18 to 75 years, male or female;
(2) Participants who met the diagnostic criteria for cervical type of colorectal cancer;
(3) Without gastrointestinal injury or abdominal operation in the sensitized detection area in the last 6 months (including trauma, acute and chronic gastroenteritis, organic injury, intestinal fistula, perforation, adhesive intestinal obstruction, etc.);
(4) With good compliance, and have signed informed consent.

Exclusion Criteria

(1) Patients complicated cardiovascular, urinary, respiratory, blood, nervous, endocrine system or other serious primary diseases who faile to effectively control the disease;
(2) Patients with skin lesions, skin allergies, skin inflammation, papules or scars under various conditions overlap with the detection area, who fail to conduct the detection;
(3) Women who are pregnant or menstruating;
(4) Participants who have been in other clinical trials within 6 months;
(5) Patients with mental disorders and intellectual disabilities, who could not cooperate to complete the questionaire.
(6) Patients with lung and other non-digestive system metastasis;

Study & Design

Study Type
Observational study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Body surface temperature;Mechanical pain threshold;
Secondary Outcome Measures
NameTimeMethod
Self-rating depression scale, SDS;Functional Assessment Cancer Therapy, FACT (V4.0);Karnofsky, KPS;Self-Rating Anxiety Scale, SAS;
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