Alternations of Intestinal Microbiota and Health Impact in CKD

NCT ID: NCT03794401

Last Updated: 2022-03-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Total Enrollment

750 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-04-01

Study Completion Date

2023-06-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This study is aimed to evaluate the impact of dietary pattern, gut microbiota and their interactions on clinical outcomes among patient with CKD stage 3-5.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Chronic Kidney Disease

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Patients with CKD stage 3-5 defined as eGFR \<60 ml/min/1.73 m2 calculated with the use of the four-variable Modification of Diet in Renal Disease formula who have not yet on dialysis therapy.

Exclusion Criteria

* Patients with active cancer
* Patients with liver cirrhosis
* Patients have taken antibiotics within three months before screening for inclusion.
* Patients with a cardiac pacemaker or metallic implants,
* Patients are amputees
* Pregnant women
* Patients with inherited renal diseases
Minimum Eligible Age

20 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Szu-Chun Hung

Attending physician

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

SZU-CHUNG HUNG

Role: PRINCIPAL_INVESTIGATOR

Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Taipei Tzu Chi Hospital

New Taipei City, , Taiwan

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Taiwan

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

TING-YUN LIN

Role: CONTACT

+886-2-66289779 ext. 2350

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Szu-Chun Hung, MD

Role: primary

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

07-XD-074

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Chinese Cohort Study of Chronic Kidney Disease
NCT03041987 ACTIVE_NOT_RECRUITING
Upper Endoscopy in CKD&ESRD
NCT04098120 UNKNOWN
CKD Cachexia and Gut Microbiome
NCT06986265 RECRUITING
Intrarenal Microvasculature in ADPKD
NCT05288998 ACTIVE_NOT_RECRUITING