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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02395484
Other study ID # MetagenomeNanjing
Secondary ID
Status Recruiting
Phase N/A
First received March 17, 2015
Last updated May 1, 2015
Start date March 2015
Est. completion date June 2016

Study information

Verified date May 2015
Source Jinling Hospital, China
Contact Ning Li, MD
Phone +86-25-80860089
Email jinlingh_lining@126.com
Is FDA regulated No
Health authority China: Food and Drug Administration
Study type Observational

Clinical Trial Summary

Constipation is a heterogeneous and multifactorial disease, influenced by a number of different genetic and environmental factors. By applying the standard two-stage GWAS strategy to design and carry out a metagenome-wide association study (MGWAS) to find the relationship between gut microbiota and constipation, to identify disease-associated metagenomic markers.


Description:

This study is a two-stage case-control metagenome-wide association study (MGWAS) based on deep next-generation shotgun sequencing of DNA extracted from the stool samples from a total of 50 Chinese constipation patients and healthy controls.


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date June 2016
Est. primary completion date March 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

1. Chronic constipation according to Rome III criteria;

2. Age = 18 years;

3. BMI: 18.5-25kg/m2;

Exclusion Criteria:

1. Bowel constipation due to innate factor (e.g. megacolon) or secondary interventions (e.g. drugs, endocrine, metabolic, neurologic or psychologic disorders);

2. History or evidence of gastrointestinal diseases (e.g. cancer, inflammatory bowel diseases);

3. Previous abdominal surgery, except cholecystectomy, appendicectomy, tubal ligation and cesarean section;

4. Previous proctological or perianal surgery;

5. Rectal prolapse and/or grade 3-4 internal hemorrhoids according to AGA classification;

6. A constipation condition meeting the Rome III criteria for IBS or functional abdominal pain syndrome;

7. Pregnant or breast-feeding women;

8. Infection with enteric pathogen;

9. Usage of probiotics, prebiotics, antibiotics or PPIs within the last month;

10. Smoking or alcohol addiction within the last 3 months;

11. Uncontrolled hepatic, renal, cardiovascular, respiratory or psychiatric disease;

12. Disease or therapy with drugs (e.g. antidepressants, opioid narcotic analgesics, anticholinergics, calcium antagonists, nitrates, antimuscarinics) that, in the opinion of the investigator, could affect intestinal transit and microbiota.

Study Design

Observational Model: Ecologic or Community, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
China Jinling Hospital Nanjing Jiangsu

Sponsors (1)

Lead Sponsor Collaborator
Jinling Hospital, China

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary taxonomic and functional characterization of gut microbiota one year No
Secondary Gut-microbiota-based constipation classification one year No
Secondary constipation-associated gut microbial markers one year No
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