Descriptive Epidemiology on Management of Mucormycosis

Mycoses Clinical Trial

Official title:

Multicenter Observational Study on Epidemiology, Treatment and Outcome of Mucormycosis in India

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03429023
• Other study ID #: FISF 001.3
• Status: Completed
• Phase: N/A
• First received: July 29, 2017
• Last updated: February 8, 2018
• Start date: April 1, 2016
• Est. completion date: September 30, 2017

Study information

• Verified date: February 2018
• Source: Fungal Infection Study Forum
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

This is an observational chart review of all patients with confirmed and probable diagnosis of mucormycosis at 19 centers across Indian hospital. Data will collect using a standardized CRF. All collected data will be entered into a database prior to analysis. Broadly data will be collected on demography, clinical characteristics, diagnosis, treatment and outcome for each patient. Patient will continue to receive treatment as per treating physicians advise. Primary outcome for this study will be overall survival at 45 & 90 days.

Description:

Introduction

Mucormycosis is a life threatening angio-invasive fungal infection generally occurring in immunocompromised individuals. In recent years the incidence has increased globally and alarmingly in India especially in patients with uncontrolled diabetes. Mucormycosis is associated with very high morbidity and mortality. Mortality can be reduced with increased awareness of the disease, and aggressive medical and surgical intervention. Though few case series of mucormycosis are published from India, multiple gaps in knowledge exist regarding epidemiology, diagnosis and management of the disease in this country. It is therefore proposed to conduct this multicentric observational study in India to evaluate epidemiology, mode of diagnosis, management practices and outcome in patients with mucormycosis.

Study Objectives

Primary:

• To describe the epidemiology, diagnosis, treatment practices and outcome of mucormycosis in India

Secondary:

• Sites involved in mucormycosis

• Underlying disease and risk factors for mucormycosis

• Spectrum of agents causing mucormycosis Ð mode of diagnosis of mucormycosis

Methods: Observation chart review Study Sites: We have assembled a network of health center across India called Mucormycosis Study Network (MSN), which consists of 19 centers across the country. Listed in Appendix 1.

Study design: We propose to conduct a single arm prospective observational study.

Study procedures:

Working definition of Proven & Probable mucormycosis used for this study. Proven case:

Presence of fungus in the tissue detected by direct microscopy (KOH, Calcoflor white) and Histopathological examination or from any aspiration /tissue from sterile site.

Probable case: Clinical features of infection in organ-site with presence of mucorale in tissue from non-sterile infected site.

Post enrollment, all patients will receive treatment as per the discretion of treating physicians or local hospital protocol. Data on patients' clinical features, risk factors, laboratory and radiological findings will be collected on standardize case report forms (CRF).

Specifically, the extent of disease will be evaluated with appropriate radiological evaluation CT scan/ MRI (Brain, PNS, Thorax, abdomen etc.) Attempt will be made to collect follow up data till 6 months after diagnosis unless the patient lost in follow up or died before six months. All culture isolates will be sent to Mycology Reference Laboratory at PGIMER, Chandigarh for final identification and drug susceptibility testing. Blocks of histopathological specimen will be sent at reference mycology laboratory for patients with histopathological diagnosis of mucormycosis for DNA extraction and species identification.

Primary outcome

1. Overall survival at 45 & 90 days

2. Cure: defined as complete resolution of clinical, radiological and mycological evidence

3. Improved: Resolution of clinical features, radiological regression

Secondary outcomes

1. Grade III and IV toxicities of antifungal agents (Refer Appendix 2 for definition)

Data Collection Data will collect using a standardized CRF. All collected data will be entered into a database prior to analysis. Broadly data will be collected on demography, clinical characteristics, diagnosis, treatment and outcome for each patient.

Patient characteristics: Demographics, Comorbidities (Diabetes, Solid organ Transplant, GVHD requiring steroids, Febrile neutropenia, prolong neutropenia + Steroid therapy, Voriconazole exposure, Immunocompetent patient, Nosocomial [Surgical site, wooden spatula, ECG lead etc], history of road traffic accidents, tsunami, hurricane, Patients receiving immunosuppressives for collagen diseases, Use of monoclonal antibodies for treatment of variety of medical conditions, Iron overload and desferioxamine therapy, Burns patients), Organ dysfunction, Bacterial super infections

Disease characteristics: Site of disease (pulmonary, PNS, Brain, skin and soft tissue, GI, Renal etc), number of lesions, species of mucormycosis

Treatment:

1. . Time to start antifungal drug after (a). Onset of disease i.e. first symptom (b). Diagnosis of mucormycosis

2. . Dose and duration of antifungal agent

3. . Time to Surgical Treatment after (a). Onset of disease i.e. first symptom (b). Diagnosis

4. . Type of Surgical treatment: Radical surgery, Debridement, Repeated debridement Adjuvant treatment used e.g. Deferasirox, posaconazole

5. . Posaconazole maintenance after completion of ABDC

Outcomes:

Overall survival (OS): OS will be measured 2 ways: from onset of first symptoms as reported by patient and from day of admission to last follow-up.

Mortality Related to mucormycosis, not related to Mucormycosis

Treatment Regimen:

The study will not interfere with management at any stage. Treating physician will determine all process of patient management including diagnosis and treatment. Information on antifungal agent used, dosage used and duration of treatment will be collected.

Information on surgical treatment will be collected i.e. time to surgical treatment after diagnosis, debridement, numbers and frequency of debridement, extensive surgical resection.

Control of diabetes, reversal of metabolic parameters, management of immunosuppression will be noted.

Follow up data will also be collected similarly.

Patients will be assessed during hospitalization for drug compliance and toxicities.

Adverse Event will be noted and graded according to standard grading system. Prior and Concomitant Therapy The details of any prior, concomitant or follow up therapy like deferasirox or Posaconazole will also be noted

Statistical Plan Patient, disease and treatment characteristics will be summarized using descriptive statistics. Differences in the primary outcome of survival according to patient, disease and treatment characteristics will be assessed using a log-rank test and illustrated using the Kaplan-Meir analysis. Differences in OS will be summarized as hazard ratio along with 95% confidence intervals (CI). Differences in mortality and toxicities according to patient, disease and treatment characteristics will summarized as risk ratio along with 95% CI. All significance testing will be two sided and set at 5%.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 500
• Est. completion date: September 30, 2017
• Est. primary completion date: September 30, 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A to 90 Years

Eligibility

Inclusion Criteria:

• All consecutive patients regardless of age with a confirmed diagnosis mucormycosis through HPE & /or culture will be enrolled in this study. In suspected cases on histopathology, molecular technique of extraction of DNA from tissue and sequencing to identify the pathogen, will be used to confirm the diagnosis

• All probable cases of mucormycosis.

Related Conditions & MeSH terms

• Mucormycosis
• Mycoses
• Zygomycosis

Locations

Country	Name	City	State
India	Sterling Hospital	Ahmedabad	Gujarat
India	St.Johns Medical College	Bangalore	Karnataka
India	PGIMER	Chandigarh
India	Sri Ramachandra Medical College & RI	Chennai	Tamil Nadu
India	Nizams Institute Of Medical Sciences	Hyderabad	Telengana
India	Christian Medical College and Hospital	Ludhiana	Panjab
India	PD Hinduja National Hospital and Medical Research centre	Mumbai	Maharashtra
India	All India Institute of Medical Sciences	New Delhi	Delhi
India	Indraprastha Apollo Hospitals	New Delhi	Delhi
India	Sir Gangaram Hospital	New Delhi	Delhi
India	VMMC and Safdarjung Hospital	New Delhi	Delhi
India	JIPMER	Pondicherry
India	Christian Medical College	Vellore	Tamil Nadu

Sponsors (2)

Lead Sponsor	Collaborator
Fungal Infection Study Forum	Mylan India Limited

Country where clinical trial is conducted

India, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Mortality	Number of deaths	Three months after the completion of the study