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Study on Optimization of clinical scheme and evaluation of curative effect of press needle in the treatment of functional constipation based on real world

Phase 1
Recruiting
Conditions
function constipation
Registration Number
ITMCTR2100004488
Lead Sponsor
Affiliated Hospital of 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

? The diagnostic criteria of functional constipation were met.
? From 18 years old to 80 years old, both male and female.
? Patients agreed to the study and signed informed consent.
Note: patients meeting the above three criteria can be included in this study.

Exclusion Criteria

1. Constipation caused by gastrointestinal dysfunction and intestinal stenosis due to organic lesions in gastrointestinal tract, such as tumor, Hirschsprung's disease, inflammatory bowel disease, peptic ulcer, cancer, and perianal diseases.
2. Patients with severe hemorrhagic disease or hypersensitivity constitution, allergic to press needle or serious adverse reactions.
3. Patients with skin damage or infection at the needling site
4. Patients with severe cognitive impairment, severe malnutrition, malignant tumor and other poor general conditions, unable to cooperate with the examination and treatment.
5. Participants in other clinical trials within 8 weeks before the start of the study.

Note: patients who meet any of the above criteria should be excluded.

Study & Design

Study Type
Interventional study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Average number of autonomous bowel movements per week;
Secondary Outcome Measures
NameTimeMethod
Cleveland Clinic Score;Bristol fecal trait score;Patient Assessment of Constipation Quality of Life Questionnaire;
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