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Cross-sectional investigation of the characterization and distribution pattern of acupoint sensitization in patients with chronic colitis

Early Phase 1
Recruiting
Conditions
chronic colitis
Registration Number
ITMCTR2024000115
Lead Sponsor
Shaanxi University of Chinese Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

Chronic colitis observation group:1) Meet the diagnostic criteria of chronic colitis;2) Sex is not limited, age between 18-65 years old;3) Those who are willing to participate in the trial and sign the informed consent.
Healthy control group:1) No chronic colitis and other digestive diseases;2) Sex is not limited, age between 18-65 years old;3) Those who are willing to participate in the trial and sign the informed consent.

Exclusion Criteria

Chronic colitis observation group: 1) does not meet the diagnostic criteria and inclusion criteria; 2) previous myocardial infarction, severe heart failure, valvular heart disease, severe arrhythmia primary cardiomyopathy, blood diseases and other serious cerebrovascular disease; 3) pregnancy, breastfeeding women and psychiatric disorders can not be cooperated with; 4) combined with intestinal tuberculosis, bacillary dysentery, malignant tumors; 5) with fever symptoms affecting thermal probe; 6) patients with skin diseases affecting shape sensitive probe; 7) patients with musculoskeletal diseases causing pain and affecting pain sensitive probe; 8) also participate in other patients with Patients with fever symptoms affecting the heat sensitivity test;
Healthy control group: 1) myocardial infarction, severe heart failure, valvular heart disease, severe arrhythmias, primary cardiomyopathy, blood diseases and other serious cerebrovascular disease; 2) pregnancy, lactation and mental illness can not cooperate with the patient; 3) combined with intestinal tuberculosis, bacterial dysentery, malignant tumors; 4) with fever symptoms affecting thermal sensitivity test; 5) patients with dermatologic diseases affecting shape sensitivity test; 6) patients with musculoskeletal diseases causing pain and affecting pain sensitivity test; 7) patients who also participate in other clinical trials.

Study & Design

Study Type
Observational study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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