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InfectionMDRNCT02140853

MDR Bacilli Surveillance and Clinical Feature in China

An observational study of Infection, run by Sun Yat-sen University at 1 site in China.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Objective 1. To evaluate the impact of MDR pathogen on prognosis and therapy cost; 2. To compare the efficacy of different antibiotics in treatment of infection caused by MDR pathogens; 3. To evaluate the risk factors of MDR pathogens infection; 4. To evaluate the distribution and characteristics of MDR pathogens; 5. Read more about this study

Who is it for?
Ages 18 to 80 years
Conditions the study is for
Infection
How many people
1,500 participants
Where
1 siteChina
Study dates
Nov 2011to Dec 2015
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: 3000

Who may be able to join

  • Gram-negative bacillus.
  • Resistant to more than 3 kinds of antibacterial agents.

Who cannot join

  • Repetitive organism isolated from the same center in one patient.
  • Judged as colonization or pollution by clinician.
  • Enrolled into other trial, and the data is not available for the current study.

Trial locations and contacts

1 site in 1 country.

Canmao Xie, MD contact

xiecanmao@163.com

Yuxing Ni, MD contact

yuxing_ni@yahoo.com.cn

China1 site, 1 recruiting
  • SunYat-senU

    Guangzhou, Guangdong, 510080

    Canmao Xie, MD, xiecanmao@163.com

    Recruiting

Other trials in China

About this study

Official title: Multi-drug Resistant Gram-negative Bacilli-surveillance and Clinical Feature in China

Objective

  1. To evaluate the impact of MDR pathogen on prognosis and therapy cost;
  2. To compare the efficacy of different antibiotics in treatment of infection caused by MDR pathogens;
  3. To evaluate the risk factors of MDR pathogens infection;
  4. To evaluate the distribution and characteristics of MDR pathogens;
  5. To investigate the proportion of MDR isolates to construct systematic database.
Read the detailed description
  1. Background: In recent years, the incidence of infection caused by multi-drug resistant (MDR) pathogen keeps increasing. The increase of MDR bacterial is a serious challenge for empirical therapy. Common empirical antibiotic may not cover MDR pathogen and is inappropriate for patients with infection caused by MDR pathogens, which finally increases mortality. A number of studies have demonstrated MDR pathogens are related to excess mortality, longer hospital stays and more treatment cost. Compared to infection caused by non-MDR pathogens, infection caused by MDR pathogens possesses higher mortality by 10% to 15%, longer ICU stays by 6 -10 days, and less appropriate empirical antibiotics by 50%. In addition, studies have shown that the treatment of infection caused by MDR pathogens is more expensive by $10,000-$50,000 than that by sensitive pathogens. Monitoring of MDR pathogens may find epidemiological trends, discover new MDR bacteria, evaluate risk factors and assess the effectiveness of interventions. Data of MDR pathogens has been available in Europe and the United States, however, is absent in China. By now, the features of bacterial resistance in different regions, hospitals, or in certain patients with exposure to antibiotics, still keep uncertainty. The current study is to enroll continuous MDR isolates and clinical data of the patients from which the pathogens were isolated. The data may clarify the distribution and characteristics of MDR pathogens in China, as well as clinical outcome of infection caused by MDR pathogens, which is essential for management and treatment of infection caused by MDR pathogens.
  2. Study center: 10
  3. Strains MDR gram-negative bacilli isolated from lower respiratory tract, pleural effusion or blood will be reported to clinician. Confirmation that the isolate is 'real' pathogen of a certain infection, not colonization or pollution, is needed. Microbiologic data will be collected, such as result of susceptibility test. Inclusion criteria:
  4. Gram-negative bacillus.
  5. Resistant to more than 3 kinds of antibacterial agents. Exclusion criteria:
  6. Repetitive organism isolated from the same center in one patient.
  7. Judged as colonization or pollution by clinician.
  8. Enrolled into other trial, and the data is not available for the current study.
  9. Microbiologic investigators collect data:
  10. General data, strain name, source department.
  11. Result of susceptibility test.
  12. Clinical data: The current trial is observational. Clinicians, rather than investigators, will decide the therapy. Clinical investigators confirm the MDR organism is not pollution or colonization by both definitions of nosocomial infection and result of semi-quantitative culture. For those eligible strains, corresponding clinical data will be collected.
  13. Demographic data. Name, gender, age and date of admission.
  14. Symptoms and signs, especially those related to infection.
  15. Laboratory result, such as blood and urine routine, biochemistry.
  16. Medical complication, especially those that influence immunity, such as diabetes, hepatic cirrhosis, malnutrition, malignancy, HIV infection or transplantation.
  17. Previous medical therapy, especially late usage of antibiotic, steroids or other immunosuppressive agents.
  18. Management of infection, including regimen and duration of antibiotic therapy, prognosis, treatment and total cost.
  19. Outcome of treatment, including efficacy at the end of antibiotic therapy and 30-day, ICU stay time, total hospital stay, and cost of antibiotic and totaltherapy cost.
  20. Sample size: Continuous MDR gram-negative bacilli and clinical data: 1500 cases. Continuous Non-MDR gram-negative bacilli and clinical data: 1500 cases.
  21. Endpoint:
  22. Mortality and therapy cost of MDR or non-MDR infection.
  23. Success rate of different antibiotics regimen for treatment of MDR infection. (Classified as 3rd and 4th cephalosporin,β-lactam and β-lactamase inhibitor compounds, carbapenems and others, monotherapy or combined therapy)
  24. Risk factors of infection caused by MDR pathogens.
  25. Resistant profile of MDR bacilli responsible for infection.
  26. Therapy cost of MDR or non-MDR infection.
  27. Statistical analysis:

Statistical analysis is conducted by t-test for continuous variables and chi-square test for categorical variables. Multivariate regression analysis, Logistic regression model is used to clarify the independent risk factors of infection and death. All p values are retained until after the decimal point two, and statistical significance was set at p <0.05.

Conditions
Infection
Keywords
MDR gram-negative bacilli, Mortality, Therapy
Medical subject headings
Infections

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT02140853
Study groupRoleWhat they receive
MDR grouppatients of MDR pathogen infection
non-MDR grouppatients of non-MDR pathogen infection

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Mortality

    Mortality comparizon between MDR or non-MDR infection

    Measured: Jun 2015

Secondary outcomes (1)
  1. Therapy cost

    Therapy cost comparizon between MDR or non-MDR infection

    Measured: Jun 2015

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted16 May 2014 (estimated)
  2. Study startNov 2011
  3. Primary completionDec 2014 (estimated)
  4. Study completionDec 2015 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case-control
Time perspective
Prospective
Enrolment
1,500 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02140853
Sponsor's protocol ID
WS1993136
Other IDs
MDR Net
Acronym
MDR
Status last verified
May 2014
First submitted
14 May 2014
Last updated
16 May 2014
Results posted
No
Data monitoring committee
Yes

Questions about this trial

What is this clinical trial studying?

An observational study of Infection, run by Sun Yat-sen University at 1 site in China.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 16 May 2014. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Canmao Xie, MD (xiecanmao@163.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Mortality (time frame: Jun 2015). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 May 2014.

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