FULL DETAILS (Read-only)  -> Click Here to Create PDF for Current Dataset of Trial
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  
Name  Address 
NIL  NIL 
 
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  
Status 
Not Applicable 
 
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.

 
Close