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.
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
Yuxing Ni, MD contact
China1 site, 1 recruiting
- Recruiting
SunYat-senU
Guangzhou, Guangdong, 510080
Canmao Xie, MD, xiecanmao@163.com
About this study
Official title: Multi-drug Resistant Gram-negative Bacilli-surveillance and Clinical Feature in China
Objective
- To evaluate the impact of MDR pathogen on prognosis and therapy cost;
- To compare the efficacy of different antibiotics in treatment of infection caused by MDR pathogens;
- To evaluate the risk factors of MDR pathogens infection;
- To evaluate the distribution and characteristics of MDR pathogens;
- To investigate the proportion of MDR isolates to construct systematic database.
Read the detailed description
- 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.
- Study center: 10
- 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:
- Gram-negative bacillus.
- Resistant to more than 3 kinds of antibacterial agents. Exclusion criteria:
- 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.
- Microbiologic investigators collect data:
- General data, strain name, source department.
- Result of susceptibility test.
- 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.
- Demographic data. Name, gender, age and date of admission.
- Symptoms and signs, especially those related to infection.
- Laboratory result, such as blood and urine routine, biochemistry.
- Medical complication, especially those that influence immunity, such as diabetes, hepatic cirrhosis, malnutrition, malignancy, HIV infection or transplantation.
- Previous medical therapy, especially late usage of antibiotic, steroids or other immunosuppressive agents.
- Management of infection, including regimen and duration of antibiotic therapy, prognosis, treatment and total cost.
- 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.
- Sample size: Continuous MDR gram-negative bacilli and clinical data: 1500 cases. Continuous Non-MDR gram-negative bacilli and clinical data: 1500 cases.
- Endpoint:
- Mortality and therapy cost of MDR or non-MDR infection.
- 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)
- Risk factors of infection caused by MDR pathogens.
- Resistant profile of MDR bacilli responsible for infection.
- Therapy cost of MDR or non-MDR infection.
- 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 group | Role | What they receive |
|---|---|---|
| MDR group | patients of MDR pathogen infection | |
| non-MDR group | patients of non-MDR pathogen infection |
What is being measured
The primary outcome is the main question the study is designed to answer.
Mortality
Mortality comparizon between MDR or non-MDR infection
Measured: Jun 2015
Secondary outcomes (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.
- First posted16 May 2014 (estimated)
- Study startNov 2011
- Primary completionDec 2014 (estimated)
- Study completionDec 2015 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for InfectionStudies of the same condition, open and under way.
- More trials run by Sun Yat-sen UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Sun Yat-sen University
- Sponsor type
- University, hospital or other
- Collaborators
- Pfizer
- Responsible party
- Principal investigator, Prof Xie Canmao, Sun Yat-sen University
- Investigators
- Canmao Xie, MD, Principal investigator, Sun Yat-sen UniversityYuxing Ni, MD, Principal investigator, Ruijin Hospital
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
Study at a glance
From the registry record, last updated by the sponsor on 16 May 2014. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Multi-drug Resistant Gram-negative Bacilli-surveillance and Clinical Feature in China
- ClinicalTrials.gov ID
- NCT02140853
- Acronym / sponsor ID
- MDR / WS1993136
- Conditions
- Infection
- Keywords
- MDR gram-negative bacilli, Mortality, Therapy
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 1,500 participants (estimated)
- Lead sponsor
- Sun Yat-sen UniversityUniversity, hospital or other
- Collaborators
- Pfizer
- Study start
- Nov 2011
- Primary completion
- Dec 2014 (estimated)
- Study completion
- Dec 2015 (estimated)
- First posted
- 16 May 2014 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Objective
- To evaluate the impact of MDR pathogen on prognosis and therapy cost;
- To compare the efficacy of different antibiotics in treatment of infection caused by MDR pathogens;
- To evaluate the risk factors of MDR pathogens infection;
- To evaluate the distribution and characteristics of MDR pathogens;
- To investigate the proportion of MDR isolates to construct systematic database.
Detailed description
- 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.
- Study center: 10
- 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:
- Gram-negative bacillus.
- Resistant to more than 3 kinds of antibacterial agents. Exclusion criteria:
- 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.
- Microbiologic investigators collect data:
- General data, strain name, source department.
- Result of susceptibility test.
- 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.
- Demographic data. Name, gender, age and date of admission.
- Symptoms and signs, especially those related to infection.
- Laboratory result, such as blood and urine routine, biochemistry.
- Medical complication, especially those that influence immunity, such as diabetes, hepatic cirrhosis, malnutrition, malignancy, HIV infection or transplantation.
- Previous medical therapy, especially late usage of antibiotic, steroids or other immunosuppressive agents.
- Management of infection, including regimen and duration of antibiotic therapy, prognosis, treatment and total cost.
- 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.
- Sample size: Continuous MDR gram-negative bacilli and clinical data: 1500 cases. Continuous Non-MDR gram-negative bacilli and clinical data: 1500 cases.
- Endpoint:
- Mortality and therapy cost of MDR or non-MDR infection.
- 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)
- Risk factors of infection caused by MDR pathogens.
- Resistant profile of MDR bacilli responsible for infection.
- Therapy cost of MDR or non-MDR infection.
- 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.
Study design
- Observational model
- Case-control
- Time perspective
- Prospective
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| MDR group | – | –patients of MDR pathogen infection |
| non-MDR group | – | –patients of non-MDR pathogen infection |
Who may qualify
- Ages
- 18 to 80 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- 3000
Key inclusion criteria (2 listed)
- Gram-negative bacillus.
- Resistant to more than 3 kinds of antibacterial agents.
Key exclusion criteria (3 listed)
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Mortality
Time frame: Jun 2015
Mortality comparizon between MDR or non-MDR infection
1 secondary outcome
Therapy cost
Time frame: Jun 2015
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 16 May 2014.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Canmao Xie, MD contact
Yuxing Ni, MD contact
Canmao Xie, MD principal investigator
Sun Yat-sen University
Yuxing Ni, MD principal investigator
Ruijin Hospital
1 site in 1 country: see every site and its status.
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.