| CTRI Number |
CTRI/2021/10/037047 [Registered on: 01/10/2021] Trial Registered Prospectively |
| Last Modified On: |
22/09/2021 |
| Post Graduate Thesis |
No |
| Type of Trial |
Interventional |
|
Type of Study
|
Drug |
| Study Design |
Randomized, Parallel Group Trial |
|
Public Title of Study
|
The effectiveness of azithromycin alone and azithromycin plus cefixime for the treatment of typhoid fever in South Asia has been studied. |
|
Scientific Title of Study
|
A comparison of concomitant administration of Azithromycin and Cefixime to Azithromycin alone in the treatment of Typhoid
|
| Trial Acronym |
ACT South Asia |
|
Secondary IDs if Any
|
| Secondary ID |
Identifier |
| NCT04349826 |
ClinicalTrials.gov |
|
|
Details of Principal Investigator or overall Trial Coordinator (multi-center study)
|
| Name |
Dr Priscilla Rupali |
| Designation |
Professor |
| Affiliation |
Christian Medical College,Vellore |
| Address |
Department of Infectous Disease,
Christian Medical College,Vellore
Vellore TAMIL NADU 632004 India |
| Phone |
04162282804 |
| Fax |
|
| Email |
priscillarupali@yahoo.com |
|
Details of Contact Person Scientific Query
|
| Name |
Dr Priscilla Rupali |
| Designation |
Professor |
| Affiliation |
Christian Medical College,Vellore |
| Address |
Department of Infectous Disease,
Christian Medical College,Vellore
Vellore TAMIL NADU 632004 India |
| Phone |
04162282804 |
| Fax |
|
| Email |
priscillarupali@yahoo.com |
|
Details of Contact Person Public Query
|
| Name |
Dr Priscilla Rupali |
| Designation |
Professor |
| Affiliation |
Christian Medical College,Vellore |
| Address |
Department of Infectous Disease,
Christian Medical College,Vellore
Vellore TAMIL NADU 632004 India |
| Phone |
04162282804 |
| Fax |
|
| Email |
priscillarupali@yahoo.com |
|
|
Source of Monetary or Material Support
|
| Award from the Joint Global Health Fund (MRC/DFID/Wellcome Trust, to the University of Oxford. |
|
|
Primary Sponsor
|
| Name |
The University of Oxford |
| Address |
The University of Oxford
University Offices
Weelington square
OXFORD
OX12JD |
| Type of Sponsor |
Research institution |
|
|
Details of Secondary Sponsor
|
|
|
Countries of Recruitment
|
Bangladesh India Nepal Pakistan |
|
Sites of Study
|
| No of Sites = 2 |
| Name of Principal
Investigator |
Name of Site |
Site Address |
Phone/Fax/Email |
| Dr Priscilla Rupali |
Christian Medical College,Vellore |
Department of Emergency Medicine, Department of Child Health, Department of Community Medicine
Ida Scudder Road
Vellore - 632004
Tamil Nadu Vellore TAMIL NADU |
04162282804
priscillarupali@yahoo.com |
| Dr Venkata Ramana |
Rural Development Trust Hospital |
Department of Medicine & Department of Peadiatrics
Kadhiri road
Bathalapalli
Ananthapuramu
Andra Pradesh Anantapur ANDHRA PRADESH |
9502261001
ramana323@gmail.com |
|
|
Details of Ethics Committee
|
| No of Ethics Committees= 2 |
| Name of Committee |
Approval Status |
| Institutional review board CMC,Vellore |
Approved |
| Institutional review board CMC,Vellore |
Approved |
|
|
Regulatory Clearance Status from DCGI
|
|
|
Health Condition / Problems Studied
|
| Health Type |
Condition |
| Patients |
(1) ICD-10 Condition: B968||Other specified bacterial agents as the cause of diseases classified elsewhere, |
|
|
Intervention / Comparator Agent
|
| Type |
Name |
Details |
| Intervention |
Azithromycin and Cefixime |
Azithromycin 20mg/kg/day- Maximum dose 1gm/day Patients 50 kg will get 1gm OD orally for for 7 days and
Cefixime Dose 20mg/kg/day
Maximum dose- 800mg/day
Patients 40 kg will get 800 mg /day orally for 7 days |
| Comparator Agent |
Azithromycin and Placebo |
Azithromycin
Dose 20 mg/kg/day
Maximum dose 1000mg/day for 7 days and
Cefixime matched placebo for 7 days
|
|
|
Inclusion Criteria
|
| Age From |
2.00 Year(s) |
| Age To |
65.00 Year(s) |
| Gender |
Both |
| Details |
1. A history of fever at presentation for 72 hours or more and a documented fever (37.5 degrees Celsius or more(axillary) or 38degree Celsius or more(oral))
2. Age 2 years or more (and weight 10kg and more) to 65 years
3.No clear focus of infection on initial clinical evaluation
4. Malaria RDT negative; dengue NS1 RDT negative; scrub typhus RDT negative; CRP rapid test 10 mg/L or more
5. Able to take oral treatment
6. Able to attend for follow-up and can be contacted by telephone
7. Written fully informed consent to participate in the study including assent for children in addition to parental/legal guardian consent.
|
|
| ExclusionCriteria |
| Details |
1. History of fever for >14 days
2. Pregnant or positive pregnancy test or breast-feeding
3. Presence of clinical symptoms or signs indicating a focal infection such as pneumonia; urinary infection, meningitis, eschar
4. Obtundation, hemodynamic shock, visible jaundice, gastrointestinal bleeding or any signs of severe disease that may require immediate hospitalization
5. Being treated for TB or HIV or severe acute malnutrition
6. Patients with cardiac disease
7. Patient requiring intravenous antibiotics for any reason
8. Previous history of hypersensitivity to any of the treatment options
9. Either of the trial drugs are contraindicated for any reason (e.g. drug interactions)
10. Has received azithromycin or cefixime in the last five days
11. Receiving another antimicrobial and responding clinically to the treatment as judged by the attending clinician.
12. Being on another drug ( for example certain kinds of antidepressants, or anticonvulsants) that may also cause prolonged QT interval
13. PCR positive for Co-Vid 19 before or after randomization
|
|
|
Method of Generating Random Sequence
|
Computer generated randomization |
|
Method of Concealment
|
Pharmacy-controlled Randomization |
|
Blinding/Masking
|
Participant, Investigator and Outcome Assessor Blinded |
|
Primary Outcome
|
| Outcome |
TimePoints |
| Clinical failure and Microbiological failure |
28 days |
|
|
Secondary Outcome
|
| Outcome |
TimePoints |
| Fever clearance time |
Under observation following the initiation of treatment |
| Time to treatment failure |
Under observation following the initiation of treatment |
| Occurrence of adverse events in each treatment arm |
Under observation following the initiation of treatment |
| Clearance of faecal carriage |
One and three month follow-up visit |
| cost-effectiveness of the treatment in |
Initiation of treatment and one month follow-up visit |
|
|
Target Sample Size
|
Total Sample Size="1500" Sample Size from India="500"
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" |
|
Phase of Trial
|
Phase 4 |
|
Date of First Enrollment (India)
|
01/10/2021 |
| Date of Study Completion (India) |
Applicable only for Completed/Terminated trials |
| Date of First Enrollment (Global) |
23/05/2021 |
| Date of Study Completion (Global) |
Applicable only for Completed/Terminated trials |
|
Estimated Duration of Trial
|
Years="3" Months="0" Days="0" |
|
Recruitment Status of Trial (Global)
|
Open to Recruitment |
| Recruitment Status of Trial (India) |
Not Yet Recruiting |
|
Publication Details
|
None yet |
|
Individual Participant Data (IPD) Sharing Statement
|
Will individual participant data (IPD) be shared publicly (including data dictionaries)?
Response - NO
|
|
Brief Summary
|
Typhoid
and paratyphoid (enteric) fever affects more than 11 million children and
adults globally each year including 7 million in South Asia. Up to 1% of
patients who get typhoid may die of the disease and,in those that survive,a
prolonged period of ill health and catastrophic financial cost to the family
may follow. In the last 20 years, treatment of typhoid fever with a 7-day
course of a single oral antimicrobial,such as ciprofloxacin, cefixime or
azithromycin, given in an out-patient setting has led to patient recovery in 4
to 6 days without the need for expensive hospitalization. Increasing antimicrobial
resistance in Asia and sub-Saharan Africa threatens the effectiveness of these treatments and increases the risk of prolonged illness and severe disease. The recent
emergence of a particularly resistant typhoid strain in Pakistan, and
subsequent international spread, adds urgency to this problem andSalmonellais
now listed as a high(Priority 2) pathogen by WHO.
Treatment with combinations of antimicrobials may be more
effective for treating typhoid fever and mitigate the problems of resistance.This suggestion is based on expert opinion but not backed up by good quality
evidence. The ACT-South Asia study aims to compare a combination of
azithromycin and cefixime with azithromycin alone in the outpatient treatment
of clinically suspected and confirmed uncomplicated typhoid fever. We will
recruit 1500 patients across sites in Bangladesh, India, Nepal and Pakistan. A
placebo (sugar pill) will be used instead of cefixime in the single drug arm so
that neither the patient nor the study team know which patient is receiving
which treatment. We will assess whether treatment outcomes are better with the
combination after one week of treatment and at one and three month follow-up.
Both antimicrobials are widely used and have excellent safety profiles. If the
combination treatment is better than the single antibiotic treatment, this will
be an important result for patients across South Asia and other typhoid endemic
areas. We will additionally investigate the financial implications for families
and health system. |