Nepal Undifferentiated Febrile Illness Trial (NUFIT)
Primary Purpose
Undifferentiated Febrile Illness
Status
Unknown status
Phase
Phase 3
Locations
Nepal
Study Type
Interventional
Intervention
Azithromycin
Co-trimoxazole
Sponsored by
About this trial
This is an interventional treatment trial for Undifferentiated Febrile Illness focused on measuring Undifferentiated febrile illness, Azithromycin, Cotrimoxazole, Efficacy, Enteric fever, Fever clearance time
Eligibility Criteria
Inclusion Criteria:
- Fever of ≥ 38.0°C and for ≥4 days without a focus of infection
- ≥ 2 years and <65 years of age
- Able to take tablets orally
- Patient residing in Kathmandu Valley
- Able to come for follow up
- Can be reached by telephone/mobile phone 24 hours a day.
- Written informed consent to participate in the study including assent for minors in addition to parental consent.
Exclusion Criteria:
- Fever >14 days
- Pregnancy
- Obtundation
- Shock
- Visible jaundice
- Presence of signs of gastrointestinal bleeding
- History of hypersensitivity to either of the trial drugs
- Patient requiring intravenous antibiotic or hospital admission for any reason.
- Contraindication of drug for any reason (e.g. drug interactions).
- Any patient fulfilling inclusion criteria but already on antimicrobials and responding clinically to the treatment
Sites / Locations
- Nepal Civil Service Hospital
- Patan Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Group A
Group B
Arm Description
Azithromycin tablets 20mg/kg/day for 7 days (Maximum dose 1000mg/day)
Co-trimoxazole tablets (Trimethoprim 10 mg/kg+Sulphamethoxazole 50 mg/kg) in two divided doses everyday for 7 days (maximum 3000mg/day)
Outcomes
Primary Outcome Measures
Fever clearance time
time from the first dose of a study drug until a temperature ≤37.5°C for at least 2 days
Secondary Outcome Measures
Fever failure
defined by fever clearance time (FCT) >7 days post treatment initiation;
Need rescue treatment
Requirement for rescue treatment as judged by the Research Medical Officer (RMO) and Attending Physician (AP)
Microbiological failure
Blood culture positivity for S. Typhi or an S. Paratyphi
Relapse
Culture-confirmed or syndromic enteric fever relapse
The development of any complication
any complication: e.g. clinically significant bleeding, fall in the Glasgow Coma Score, perforation of the gastrointestinal tract and hospital admission
Time-to-treatment failure
the time from the first dose of treatment until the date of the earliest failure event
Adverse events
grade 3/4 adverse events, serious adverse events, adverse events of any grade leading to modification of study drug dose or interruption/early discontinuation
Full Information
NCT ID
NCT02773407
First Posted
May 5, 2016
Last Updated
August 27, 2019
Sponsor
Oxford University Clinical Research Unit, Vietnam
Collaborators
University of Oxford, Wellcome Trust
1. Study Identification
Unique Protocol Identification Number
NCT02773407
Brief Title
Nepal Undifferentiated Febrile Illness Trial
Acronym
NUFIT
Official Title
Parallel Group, Double Blinded, 1:1, Randomized Controlled Phase III Trial of Co-trimoxazole Versus Azithromycin for the Treatment of Undifferentiated Fever In Nepal
Study Type
Interventional
2. Study Status
Record Verification Date
April 2018
Overall Recruitment Status
Unknown status
Study Start Date
May 23, 2016 (Actual)
Primary Completion Date
August 4, 2019 (Actual)
Study Completion Date
August 4, 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Oxford University Clinical Research Unit, Vietnam
Collaborators
University of Oxford, Wellcome Trust
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of the study is to determine whether azithromycin or cotrimoxazole is the best empirical treatment for undifferentiated febrile illness in Nepal
Detailed Description
Fever is one of the most common presenting symptoms of patients presenting to health centers in Nepal. Many of the times, it is difficult to diagnose the cause of the fever by initial history, clinical examination and basic laboratory tests and the patents are treated as presumed enteric fever or fever without focus needing antimicrobials. In fact there are various causes of similarly presenting febrile illnesses including typhoid, paratyphoid, murine typhus, scrub typhus etc.
Many of the traditionally used drugs including fluoroquinolones are now resistant against enteric fever in south asia. Oral azithromycin is now commonly used to treat undifferentiated febrile illness and remains effective against enteric fever. Many physicians now also use co-trimoxazole as it was very commonly used in the treatment of enteric fever in the past. Resistance to co-trimoxazole emerged two decades ago, but has subsequently largely disappeared and nearly all Salmonella Typhi and Paratyphi A strains from Nepal are now susceptible. Anecdotal reports claim that it seems to work very well against undifferentiated febrile illness in Nepal; it is largely stocked in government health facilities and is a popular and cheap treatment option.
Both azithromycin and co-trimoxazole are available in Nepal and are extensively used in the treatment of undifferentiated febrile illness. Therefore it is important to know the better oral option to treat enteric fever and other febrile illnesses and also to have an alternative oral treatment in case resistance to azithromycin emerges.
The investigators purpose to conduct a head to head, parallel group, 1:1, double blinded randomized controlled trial to compare azithromycin and co-trimoxazole for the treatment of undifferentiated febrile illness and determine the best empirical treatment for undifferentiated febrile illness in Nepal.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Undifferentiated Febrile Illness
Keywords
Undifferentiated febrile illness, Azithromycin, Cotrimoxazole, Efficacy, Enteric fever, Fever clearance time
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
330 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Group A
Arm Type
Active Comparator
Arm Description
Azithromycin tablets 20mg/kg/day for 7 days (Maximum dose 1000mg/day)
Arm Title
Group B
Arm Type
Active Comparator
Arm Description
Co-trimoxazole tablets (Trimethoprim 10 mg/kg+Sulphamethoxazole 50 mg/kg) in two divided doses everyday for 7 days (maximum 3000mg/day)
Intervention Type
Drug
Intervention Name(s)
Azithromycin
Intervention Type
Drug
Intervention Name(s)
Co-trimoxazole
Primary Outcome Measure Information:
Title
Fever clearance time
Description
time from the first dose of a study drug until a temperature ≤37.5°C for at least 2 days
Time Frame
at least 2 days
Secondary Outcome Measure Information:
Title
Fever failure
Description
defined by fever clearance time (FCT) >7 days post treatment initiation;
Time Frame
over 7 days post treatment initiation
Title
Need rescue treatment
Description
Requirement for rescue treatment as judged by the Research Medical Officer (RMO) and Attending Physician (AP)
Time Frame
within 63 days
Title
Microbiological failure
Description
Blood culture positivity for S. Typhi or an S. Paratyphi
Time Frame
on day 7 of treatment
Title
Relapse
Description
Culture-confirmed or syndromic enteric fever relapse
Time Frame
within 28 days of initiation of treatment
Title
The development of any complication
Description
any complication: e.g. clinically significant bleeding, fall in the Glasgow Coma Score, perforation of the gastrointestinal tract and hospital admission
Time Frame
within 28 days of initiation of treatment
Title
Time-to-treatment failure
Description
the time from the first dose of treatment until the date of the earliest failure event
Time Frame
within 63 days
Title
Adverse events
Description
grade 3/4 adverse events, serious adverse events, adverse events of any grade leading to modification of study drug dose or interruption/early discontinuation
Time Frame
within 63 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Fever of ≥ 38.0°C and for ≥4 days without a focus of infection
≥ 2 years and <65 years of age
Able to take tablets orally
Patient residing in Kathmandu Valley
Able to come for follow up
Can be reached by telephone/mobile phone 24 hours a day.
Written informed consent to participate in the study including assent for minors in addition to parental consent.
Exclusion Criteria:
Fever >14 days
Pregnancy
Obtundation
Shock
Visible jaundice
Presence of signs of gastrointestinal bleeding
History of hypersensitivity to either of the trial drugs
Patient requiring intravenous antibiotic or hospital admission for any reason.
Contraindication of drug for any reason (e.g. drug interactions).
Any patient fulfilling inclusion criteria but already on antimicrobials and responding clinically to the treatment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Buddha Basnyat, MBBS,MSc,MD
Organizational Affiliation
University of Oxford
Official's Role
Principal Investigator
Facility Information:
Facility Name
Nepal Civil Service Hospital
City
Kathmandu
Country
Nepal
Facility Name
Patan Hospital
City
Kathmandu
Country
Nepal
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
Anonymised individual participant data will be made available to researcher and public as a supporting material via open access journal and/or upon request by qualified research groups
Citations:
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Citation
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Nepal Undifferentiated Febrile Illness Trial
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