Comparative Efficacy of Single-dose Doxycycline Versus Standard 5- Day Amoxicillin Treatment
Primary Purpose
Fever
Status
Completed
Phase
Phase 4
Locations
Senegal
Study Type
Interventional
Intervention
Doxycycline
Amoxicillin
Sponsored by
About this trial
This is an interventional treatment trial for Fever
Eligibility Criteria
Inclusion Criteria:
- Participants over 8 years with no malaria fever
Exclusion Criteria:
Under 8 years Pregnanants women
-
Sites / Locations
- Niakhar observational site
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
subjects treated with doxycycline
subjects treated with amoxycilline
Arm Description
The participants treated by doxycycline 100 mg will have one dose but followed 5 days
The participants treated with amoxycilline 500 mg will have 2 doses per days during 5 days treatement and follwed during these 5 days
Outcomes
Primary Outcome Measures
Non-inferiority comparison of the efficacy between Doxycycline and Amoxicillin after 7 days of follow-up
The endpoint was cure at day-7 post-inclusion. Clinical cure was defined as a body temperature < 37.5°C. Clinical failure was defined as persistence of fever > 37.5°C at day-7. The investgators used a non-inferiority margin of 10%.
Secondary Outcome Measures
Full Information
NCT ID
NCT03765931
First Posted
June 20, 2018
Last Updated
December 4, 2018
Sponsor
Institut de Recherche pour le Developpement
1. Study Identification
Unique Protocol Identification Number
NCT03765931
Brief Title
Comparative Efficacy of Single-dose Doxycycline Versus Standard 5- Day Amoxicillin Treatment
Official Title
Comparative Efficacy of Single-dose Doxycycline Versus Standard 5- Day Amoxicillin Treatment for Patients With Non-malarial Fever: a Randomized Non-inferiority Trial in Senegal
Study Type
Interventional
2. Study Status
Record Verification Date
December 2018
Overall Recruitment Status
Completed
Study Start Date
July 2016 (undefined)
Primary Completion Date
January 2017 (Actual)
Study Completion Date
October 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Institut de Recherche pour le Developpement
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Abstract: Background The current practice in Senegal is to use broad-spectrum antibiotics including amoxicillin and/or cotrimoxazole in case of non-malarial fevers. First-line treatment with doxycycline has cured such patients. The investgators aimed to determine the efficacy of a single dose of doxycycline compared to a 5-day amoxicillin course for the treatment of fever.
Detailed Description
Methods The investgators conducted a non-inferiority, open-label, randomized controlled trial in patients aged > 8 years recruited from dispensaries in the rural area of Niakhar, Senegal. Participants were enrolled based on a body temperature > 37.5°C, as assessed using an electronic axillary thermometer. Febrile patients with a positive malaria test were excluded from the study. Participants were randomly assigned (1:1) to receive either a single dose of doxycycline (30 mg/kg) or a five-day course of amoxicillin (20 mg/kg) by a computer-generated random number sequence. The investgators monitored participants at days 2 and 7 post-treatment. The primary outcome was cure after 7 days, defined as a body temperature < 37.5°C. The investgators used a non-inferiority margin of 10%. This trial was approved by the national ethic committees of the Senegalese Ministry of Health in May 2017 (0026/MSAS/DPRS/CNERS, March, 7, 2016).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fever
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
We aimed to determine the efficacy of a single dose of doxycycline compared to a 5-day amoxicillin course for the treatment of fever.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
274 (Actual)
8. Arms, Groups, and Interventions
Arm Title
subjects treated with doxycycline
Arm Type
Active Comparator
Arm Description
The participants treated by doxycycline 100 mg will have one dose but followed 5 days
Arm Title
subjects treated with amoxycilline
Arm Type
Placebo Comparator
Arm Description
The participants treated with amoxycilline 500 mg will have 2 doses per days during 5 days treatement and follwed during these 5 days
Intervention Type
Drug
Intervention Name(s)
Doxycycline
Intervention Description
The investigators conducted a non-inferiority, open-label, randomized controlled trial in patients aged > 8 years recruited from dispensaries in the rural area of Niakhar, Senegal. Participants were enrolled based on a body temperature > 37.5°C, as assessed using an electronic axillary thermometer. Febrile patients with a positive malaria test were excluded from the study. Participants were randomly assigned (2:1) to receive either a single dose of doxycycline (30 mg/kg) or a five-day course of amoxicillin (20 mg/kg) by a computer-generated random number sequence. The investigators monitored participants at days 2 and 7 post-treatment. The primary outcome was cure after 7 days, defined as a body temperature < 37.5°C.
Intervention Type
Drug
Intervention Name(s)
Amoxicillin
Intervention Description
The investigators conducted a non-inferiority, open-label, randomized controlled trial in patients aged > 8 years recruited from dispensaries in the rural area of Niakhar, Senegal. Participants were enrolled based on a body temperature > 37.5°C, as assessed using an electronic axillary thermometer. Febrile patients with a positive malaria test were excluded from the study. Participants were randomly assigned (2:1) to receive either a single dose of doxycycline (30 mg/kg) or a five-day course of amoxicillin (20 mg/kg) by a computer-generated random number sequence. The investigators monitored participants at days 2 and 7 post-treatment. The primary outcome was cure after 7 days, defined as a body temperature < 37.5°C.
Primary Outcome Measure Information:
Title
Non-inferiority comparison of the efficacy between Doxycycline and Amoxicillin after 7 days of follow-up
Description
The endpoint was cure at day-7 post-inclusion. Clinical cure was defined as a body temperature < 37.5°C. Clinical failure was defined as persistence of fever > 37.5°C at day-7. The investgators used a non-inferiority margin of 10%.
Time Frame
7 days follow up
10. Eligibility
Sex
All
Minimum Age & Unit of Time
8 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Participants over 8 years with no malaria fever
Exclusion Criteria:
Under 8 years Pregnanants women
-
Facility Information:
Facility Name
Niakhar observational site
City
Niakhar
State/Province
Fatick
Country
Senegal
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
Will share by restitution with the communuty
IPD Sharing Time Frame
Just after close out and analysing the data
IPD Sharing Access Criteria
Share with participants but also with the ministry of heath
Learn more about this trial
Comparative Efficacy of Single-dose Doxycycline Versus Standard 5- Day Amoxicillin Treatment
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