Functional Constipation
Conditions
Interventions
Treatment group:Lactulose+moxibustion
control group:Lactulose+comfort moxibustion
Sponsors
General Hospital of the Western Theater of the Chinese People's Liberation Army
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: ? Meets the diagnostic criteria of Western medicine for functional constipation; ? Qi deficiency constipation patients; ? Between the ages of 18 and 70; ? Excluding constipation secondary to organic diseases; ? The subject must have informed consent and voluntarily accept and cooperate with this trial treatment plan; ? The subjects have the ability to make independent judgments and express themselves in language; ? Subject can lie on their side for a long time (>30 minutes)
Exclusion criteria
Exclusion criteria: ? Those who do not meet the inclusion criteria mentioned above; ? Those with severe diseases of important organs such as the heart, brain, lungs, liver, and kidneys; ? Individuals who have taken traditional Chinese medicine, Western medicine, and probiotics for the treatment of this disease within one month prior to inclusion in the trial; ? Participants in other clinical trials within one month prior to inclusion in the trial; ? Patients with severe skin diseases; ? Those who are prohibited from using lactulose oral liquid; ? Diarrhea confirmed through investigation to be caused by infectious diarrhea, inflammatory bowel disease, hyperthyroidism, malignant tumors, and other diseases; ? Pregnant or lactating patients
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Intestinal flora;Score of bowel movements;Bristol score; | — |
Secondary
| Measure | Time frame |
|---|---|
| Quality of life scale (PAC-QOL) score of constipation patients;SDS score;SAS score;Symptom Checklist Score for Constipation Patients (PAC-SYM Score); | — |
Countries
China
Contacts
Public ContactPang Rizhao
General Hospital of the Western Theater of the Chinese People's Liberation Army
Outcome results
None listed