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New approach and key technology for Chronic constipation diagnosis base on bionic assessment

New approach and key technology for Chronic constipation diagnosis base on bionic assessment

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300078807
Enrollment
Unknown
Registered
2023-12-19
Start date
2023-12-20
Completion date
Unknown
Last updated
2024-01-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

chronic constipation

Interventions

Experimental group :none
Control group:none

Sponsors

Army Medical Center( Daping Hospital)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Patients gave informed consent and volunteered to participate in this study; (2) Male or female, subject age between 18 and 70 years old; (3) Healthy subjects: asymptomatic healthy individuals; (4) Chronic constipation patients: meeting the Rome IV diagnostic criteria for functional constipation and the diagnostic criteria for pelvic floor functional defecation disorders; (5) No history of rectal-anal surgery, untreated by medication or poorly treated by medication.

Exclusion criteria

Exclusion criteria: (1) Subject age = 18 years or subject age = 70 years; (2) Definite cause of secondary constipation and pharmacogenetic constipation; (3) Atopic infections (e.g., tuberculosis, Crohn's disease, ulcerative colitis, etc.); (4) Organic diseases of the gastrointestinal tract or other systemic diseases involving the gastrointestinal tract, such as neuromuscular lesions, endocrine and metabolic diseases, systemic sclerosis, and neurological diseases; (5) Those with a combination of serious primary diseases of the cardiovascular, cerebrovascular, hepatic, renal, respiratory and hematopoietic systems, malignant tumors and/or other progressive underlying diseases; (6) Women who are pregnant, lactating, or in a special physiological cycle; (7) Uncooperative or mentally abnormal patients; (8) Patients with other factors that may affect the results of the study or who, in the judgment of the investigator, should not be admitted to the study.

Design outcomes

Primary

MeasureTime frame
Constipation Rating System Scale;Visual Analog Scale for Pain;Patient Assessment of Quality of Life Questionnaire for Constipation;Fecobionics evaluation;

Secondary

MeasureTime frame
Anorectal manometry;Defecography;

Countries

China

Contacts

Public ContactYang Min

Army Medical Center

yangmindoctor@126.com+86 189 8309 8877

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 9, 2026