Invasive Mould Infections in Indian ICUs - Descriptive Epidemiology, Management and Outcome
NCT ID: NCT02683642
Last Updated: 2018-02-08
Study Results
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.
COMPLETED
420 participants
OBSERVATIONAL
2016-04-30
2017-09-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Due these limitations in diagnosis, there is no uniform management protocol in ICUs of India. To develop optimal management protocol, we need to know the epidemiology, the right patient to treat, antifungal drug resistance, optimal drug and duration of therapy etc. The present study will provide descriptive epidemiology, present status of diagnosis and management practiced in India to treat IMIs in ICUs. This will help to find the suitable intervention strategies to improve outcome of IMIs in India.This descriptive observational prospective study will document the epidemiologic and clinical characteristics, as well as treatment and outcome data, of patients with IMIs in ICUs in India over one year.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Characterization of Fungal Infections in COVID-19 Infected and Mechanically Ventilated Patients in ICU
NCT04368221
Multi-center Observational Study to Evaluate Epidemiology and Resistance Patterns of Common ICU-Infections (MOSER)
NCT01346735
Performance of Clinical and Biological Diagnostic Tests in Reference to the Recommended Tests for the Management of Fungal Peritonitis in Intensive Care
NCT03973645
Invasive Pulmonary Aspergillosis and Severe Influenza
NCT04232956
Staging Candidiasis in ICU Patients
NCT01322698
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Methods
Study description: Prospective, multicenter study in iCUs in India.
Purpose: Determination of epidemiologic parameters, including risk factors, description of current management and outcome of patients with IMI will be recorded prospectively. The study will help in understanding the epidemiology of IMI in ICUs and possible planning for future management strategies for IMI specific to India.
Risk: There is no risk to the patient from the study as it is only an observational study and no intervention is intended.
Site selection: 15 ICU's are identified across the country where ICU physicians are well versed about invasive fungal infections and competent diagnostic mycology laboratory is available
A site feasibility survey was conducted. This ensured that participating sites fulfill the following inclusion criteria: a) maintains ICD coding and total number of discharges and deaths at the center; b) manages critically ill patients in ICU; c) has access to high-resolution CT (HRCT) scans; d) has a mycology laboratory that performs isolation and identification of fungi at least perform galactomannan test; and e) has histopathology facilities.
Study Period: April 1, 2016 to June 30, 2017. Case enrolment - April 1, 2016 to March 31, 2017. Analysis of data - April 1, 2017 to June 30, 2017
No. of patients: All consecutive patients with proven and probable IMI in ICUs at the study centers during the study period will be included.
Patient selection All consecutive patients diagnosed for proven or probable IMIs in ICUs at the study sites will be included.
Inclusion criteria:
Proven:
Histopathology/cytology/culture/direct microscopy demonstrating septate hyphae invading tissue or aspirate from sterile sites
Probable:
* Host satisfies host criteria of EORTC
* Host with COPD satisfying definitions by Bulpa P, et al Eur Resp J 2007
* Host in ICU satisfying clinical algorithm by Blot SI, et al Am J Resp Crit Care Med 2012
Exclusion criteria:
* Endemic mycoses (histoplasmosis, sporotrichosis, penicilliosis)
* Yeast infections
* Allergic fungal diseases like allergic bronchopulmonary aspergillosis
* Infection limited to the skin only
Conduct of the study
Investigators of the study: Arunaloke Chakrabarti will be the coordinator of the study. Each site will have a Principal Investigator - the site PI. Other investigators at the site will be co-investigators.
Patient enrollment: The site PI (or one of the co-investigators) will review the patient's paper and electronic records to determine if the patient satisfies the inclusion criteria. Patients who fulfill the inclusion criteria will be included as a case.
Data collection: The demographic, clinical, treatment and outcome data will be collected by investigator and email the form to the study coordinator, Arunaloke Chakrabarti. Outcome will be measured on day of discharge/death/30 and 120 days (whichever is earlier) after the diagnosis of the IMI. The date of diagnosis of an IMI is the day on which the diagnosis is defined as proven or probable. For cases that were enrolled as probable but subsequently became proven, the date of diagnosis is the earlier date. In addition, each center will also obtain data from its relevant hospital authority on the total number of discharges and deaths in ICUs for the period of April 1, 2016 to March 31, 2017.
Fungal isolates: All isolates from proven and probable IMIs will be sent to Mycology Reference Laboratory at PGIMER, Chandigarh for final identification and antifungal susceptibility testing
Patient management: The study will not interfere with patient management.
Statistics
The study will be analyzed using descriptive statistics. It is anticipated that the study will provide the following information:
* Incidence of IMI among patients in ICUs during the study period in the participating centers
* Relative frequency of each risk factor among IMI patients at the participating centers.
* Three-month survival of patients diagnosed with IMI.
* Other data the study should be able to generate will be in accordance with the objectives.
* Kaplan-Meier plots will be used to describe the survival of patients with IMI according to their underlying diagnosis.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
OTHER
PROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Histopathology/cytology/culture/direct microscopy demonstrating septate hyphae invading tissue or aspirate from sterile sites
Probable:
* Host criteria of EORTC
* Host with COPD satisfying definitions by Bulpa P, et al Eur Resp J 2007
* Host in ICU satisfying clinical algorithm by Blot SI, et al Am J Resp Crit Care Med 2012
Exclusion Criteria
* Yeast infections
* Allergic fungal diseases like allergic bronchopulmonary aspergillosis
* Infection limited to the skin only
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Merck Sharp & Dohme LLC
INDUSTRY
Fungal Infection Study Forum
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Arunaloke Chakrabarti
Chairman, FISF
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Arunaloke Chakrabarti, MD, DNB
Role: STUDY_DIRECTOR
PGIMER, Chandigarh
Shivaprakash M Rudramurthy, MD
Role: PRINCIPAL_INVESTIGATOR
PGIMER, Chandigarh
Randeep Guleria, MD
Role: PRINCIPAL_INVESTIGATOR
AIIMS, New Delhi
Malini Capoor, MD
Role: PRINCIPAL_INVESTIGATOR
Vardhman Mahavir Medical College, New Delhi
Arvind Baronia, MD
Role: PRINCIPAL_INVESTIGATOR
SGPGI, Lucknow
Subhash Todi, MD
Role: PRINCIPAL_INVESTIGATOR
AMRI Hospitals, Kolkata
Sanjay Bhattacharyya, MD
Role: PRINCIPAL_INVESTIGATOR
Tata Medical Centre, Kolkata
P Umabala, MD
Role: PRINCIPAL_INVESTIGATOR
NIMS, Hyderabad
Ranganathan Iyer, MD
Role: PRINCIPAL_INVESTIGATOR
Global Hospital, Hyderabad
Ram Gopalakrishnan, MD
Role: PRINCIPAL_INVESTIGATOR
Apollo Hspital, Chennai
Anupma J Kindo, MD
Role: PRINCIPAL_INVESTIGATOR
Sri Ramchandra Medical University, Chennai
O C Abraham, MD
Role: PRINCIPAL_INVESTIGATOR
CMC, Vellore
Sriram Sampath, MD
Role: PRINCIPAL_INVESTIGATOR
St John Medical College, Bengaluru
Rajeev Soman, MD
Role: PRINCIPAL_INVESTIGATOR
Hinduja Hospital, Mumbai
Atul Patel, MD
Role: PRINCIPAL_INVESTIGATOR
Sterling Hospital, Ahmedabad
Pradip Bhattacharyya, MD
Role: PRINCIPAL_INVESTIGATOR
Chirayu Medical College, Bhopal
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Sterling Hospital
Ahmedabad, Gujarat, India
St.Johns Medical College
Bangalore, Karnataka, India
Chirayu Medical College
Bhopal, Madhya Pradeh, India
Tata Memorial Hospital
Mumbai, Maharashtra, India
Sir Gangaram Hospital
New Delhi, National Capital Territory of Delhi, India
Indraprastha Apollo Hospitals
New Delhi, National Capital Territory of Delhi, India
Sri Ramchandra Medical university
Chennai, Tamil Nadu, India
Christian Medical College
Vellore, Tamil Nadu, India
Nizams Institute Of Medical Sciences
Hyderabad, Telangana, India
AMRI Hospital
Kolkata, West Bengal, India
PGIMER
Chandigarh, , India
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Chakrabarti A, Kaur H, Savio J, Rudramurthy SM, Patel A, Shastri P, Pamidimukkala U, Karthik R, Bhattacharya S, Kindo AJ, Bhattacharya P, Todi S, Gopalakrishan R, Singh P, Pandey A, Agarwal R. Epidemiology and clinical outcomes of invasive mould infections in Indian intensive care units (FISF study). J Crit Care. 2019 Jun;51:64-70. doi: 10.1016/j.jcrc.2019.02.005. Epub 2019 Feb 5.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
FungalISF
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.