Establish and Apply the Evaluation System of Ultrasonic Integrated Technology for Prevention and Treatment of Acute Kidney Injury

November 23, 2023 updated by: RenJi Hospital
Establish an integrated evaluation system of ultrasound technology for the prognosis of acute kidney injury, and in order to achieve non-invasive, reliable early diagnosis "gold standard". Set up collabration with the expert in National Cheng Kung University Medical Center of Taiwan who did a lot of excellent work in basic research of prevention the progression of acut kidney injury. Study the experience about prevention progression of kidney disease in clinical and basic field. Establish cooperation with the professional in Hong Kong University of Science and Technology. To set up the system of natural products research and assess the Astragalus medicinal value.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Actual)

196

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

  • China
    • Shanghai
      • Shanghai, Shanghai, China, 200127
        • Department of nephrology , Ren Ji Hospital, Shanghai Jiao Tong University School of Medicine

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 80 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Sampling Method

Probability Sample

Study Population

Confirmed acute kidney injury

Description

Inclusion Criteria:

  • Subjects must satisfy the following criteria to be enrolled in the study:

    1. Clinical diagnosis of acute or chronic kidney injury
    2. Male or female, aged 18-80 years old
    3. signed informed consent
    4. Patients can breathe in, breathe out and hold their breathe with ease, communication without difficulty.

Exclusion Criteria:

  • Potential subjects who meet any of the following criteria will be excluded from participating in the study:

    1. Refuse to sign informed consent
    2. allergy to micro bubble hexafluoride drug
    3. Patients with cardiopulmonary insufficiency, pleural effusion, pulmonary infections
    4. Patients with asthma, chronic bronchitis
    5. Patients with pregnancy
    6. Patients can't cooperate or have a difficulty in breathing in, breathing out or holding their breathe
    7. Patients beening diagnosed with End-stage kidney disease.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Confirmed acute kidney injury
Other: kidney ultrasound
kidney ultrasound

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
compare the results of kidney ultrasound with biomarkers of acute kidney injury
Time Frame: up to 24 months
up to 24 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

RenJi Hospital

Collaborators

National Cheng-Kung University Hospital
China-Japan Friendship Hospital

Investigators

  • Principal Investigator: shan mou, Dr., Ren Ji Hospital, Shanghai Jiao Tong University School of Medicine

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

April 1, 2014

Primary Completion (Actual)

November 15, 2017

Study Completion (Actual)

December 30, 2017

Study Registration Dates

First Submitted

January 22, 2015

First Submitted That Met QC Criteria

January 27, 2015

First Posted (Estimated)

January 28, 2015

Study Record Updates

Last Update Posted (Actual)

November 27, 2023

Last Update Submitted That Met QC Criteria

November 23, 2023

Last Verified

November 1, 2023

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 2014DFT30090

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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