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1H NMR-based metabolic profiling study on acupuncture treating for functional intestinal disorders

1H NMR-based metabolic profiling study on acupuncture treating for functional intestinal disorders

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-13003537
Enrollment
Unknown
Registered
2013-08-24
Start date
2013-09-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Functional Intestinal Disorders

Interventions

A (Patient with coprostasis):Acupuncture
B (Patient with coprostasis):Sham Acupuncture
A (Patient with Diarrhea):Acupuncture
B (Patient with Diarrhea):Sham Acupuncture

Sponsors

Chengdu University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 30 Years

Inclusion criteria

Inclusion criteria: 1. Functional intestinal disorders patients inclusion criteria: The patients who meet the following inclusion criteria will be included in this study. The criteria are: (1) diagnosed with functional constipation, functional diarrhea and irritable bowel syndrome with diarrhea or constipation according to the Rome III Diagnostic Criteria; (2) aged between 18 and 30 years old, body mass index (BMI) between 18 and 24; (3) without using gastrointestinal dynamic drugs in the 15 days before enrollment, without taking part in any other clinical trials; (4) local patients or reside in local over a year; 5)provide a written informed consent. 2. Healthy volunteers inclusion criteria: Healthy volunteers who fulfill the following inclusion criteria will be included in this study. The criteria are: (1) without functional or organic diseases in the study for a year; (2) aged between 20 and 30 years old, BMI between 18 and 24; (3) without using gastrointestinal dynamic drugs in the 15 days before enrollment, without taking part in any other clinical trials; (4) local patients or reside in local over a year; (5) provide a written informed consent.

Exclusion criteria

Exclusion criteria: Patients with any of the following conditions will be excluded: 1. unconsciousness or psychopath; 2. clinical biochemical abnormalities, advanced malignant tumors or others serious wasting diseases, easy to infection or bleeding disorders; 3. suffering from any significant health problem of the heart, liver, kidney, digestion, or hematopoietic system, or other severe diseases; 4. pregnant women or women in lactation; 5. having a history of substance abuse, alcoholism or smoker.

Design outcomes

Primary

MeasureTime frame
The number of times of defecation during per week;

Secondary

MeasureTime frame
Shape and properties of stool by using Bristol Sha;Constipation Scoring System, CSS;the MOS item Short From health survey, SF-36;Self-Rating Anxiety Scale, SAS; Self-rating Depressi;Diet review and record;

Countries

China

Contacts

Public ContactLi Ying
jialee@mail.sc.cninfo.net+86 13708095607

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026