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The effect of the therapy of 'combination three methods progression' in patients with neurogenic bowel dysfunction (constipated type): study protocol for a randomized controlled trial

Phase 1
Recruiting
Conditions
neurogenic bowel dysfunction (constipated type)
Registration Number
ITMCTR2100004571
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

(1) Patients with spinal cord injury diagnosed by CT or MRI who meet the 2011 edition of the American Spinal Injury Association (ASIA) International Standard for Neurological Classification of Spinal Cord Injury: Grades B to D;or meet the diagnostic criteria for cerebral haemorrhage in the 2014 edition of the Chinese Guidelines for the Diagnosis and Treatment of Cerebral Haemorrhage, confirmed by CT or MRI; or meet the diagnostic criteria for cerebral infarction in the 2017 edition of the Chinese Guidelines for the Diagnosis and Treatment of Cerebral Infarction with Integrative Medicine, confirmed by CT or MRI.
(2) meet the Roman ? diagnostic criteria for functional constipation;
(3) aged 20-80 years;
(4) with stable vital signs, clear consciousness and normal communication and expression skills;
(5) who sign the informed consent form and submit to the arrangements of the subject group.
Note: Only patients who meet the above 5 criteria can be included in this study.

Exclusion Criteria

(1) Patients with combined serious primary diseases of the heart, liver, kidney and endocrine system;
(2) Pregnant and lactating patients;
(3) Patients with severe clotting disorders;
(4) Patients with psychiatric disorders;
(5) Patients with skin allergies or breakout the treated area;
(6) Patients who have already participated in other clinical trials.
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
umber of spontaneous bowel movements(SBMs) per week;
Secondary Outcome Measures
NameTimeMethod
GSES;Stool character typing ;SAS;Degree of difficulty in defecation;SDS;
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