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Therapeutic effect of percutaneous electroacupuncture combined with adaptive biofeedback in the treatment of outlet obstructive constipatio

Not Applicable
Conditions
outlet obstructed constipation
Registration Number
ITMCTR2000003814
Lead Sponsor
Anhui Provincial Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

1. There was evidence of outlet obstruction and met Rome IV diagnostic criteria for functional constipation
2. Aged 18 to 65 years old male and female;
3. Colonoscopy was performed in a Grade-A hospital one year before the enrollment to exclude intestinal cancer, ulcer, inflammation or other organic intestinal diseases;
4. B-ultrasound examination was performed in a Grade-A hospital one year before admission to exclude hepatobiliary and pancreatic diseases;
5. The patients with normal ECG examination in our center one month before admission (QT interval was within normal range).

Exclusion Criteria

1. Have a history of abdominal surgery;
2. Organic diseases of digestive system (including polyps, inflammatory bowel disease, tumor, celiac disease, lactose intolerance, etc.);
3. Any antispasmodic and analgesic drugs, gastrointestinal motility drugs, acid inhibitors, microecological agents, antibiotics, antidepressants, etc. were used within 2 weeks before enrollment;
4. B ultrasound examination of liver, gallbladder and pancreas diseases;
5. People with hypertension and unstable blood pressure control;
6. Patients with diabetes mellitus, thyroid disease, systemic sclerosis, systemic lupus erythematosus, etc;
7. Patients with severe psychological disorders;
8. pregnant women, lactating women or planned pregnancies;
9. There are allergic patients taking polyethylene glycol 4000 powder;
10. Observation contents:
(1) Basic information collection;
(2) Constipation symptom severity score pac-sym;
(3) Constipation quality of life score pac-qol;
(4) Anal sphincter pressure during defecation;
(5) Changes of serum psychosomatic neurotransmitters (conditional units).

Study & Design

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