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Antibiotic Prophlaxis for High-risk Laboring Women in Low Income Countries

Primary Purpose

Postpartum Sepsis, Postpartum Endometritis, Postpartum Fever

Status
Completed
Phase
Phase 4
Locations
Cameroon
Study Type
Interventional
Intervention
Azithromycin
Azithromycin and amoxicillin
Placebo
Sponsored by
University of Alabama at Birmingham
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Postpartum Sepsis

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Women ≥ 37 weeks' viable singleton or twin gestation in labor planning a vaginal delivery with

    1. Prolonged membrane rupture (≥8 hours) or
    2. Prolonged labor (≥18 hours).

Exclusion Criteria:

  • Clinical chorioamnionitis or any other active bacterial infection (e.g. pyelonephritis, pneumonia, abscess) at time of randomization: because standard antibiotic therapy for these conditions may confound trial intervention.
  • Allergy to azithromycin or amoxicillin
  • Plan for cesarean delivery prior to enrollment
  • Fetal demise or major congenital anomaly: Major congenital anomalies may confound assessment of neonatal outcomes and every attempt will be made up front to exclude them from randomization. However, some unrecognized fetal anomalies may inevitably be randomized. These will not be excluded post-randomization from the primary (maternal outcome) analysis; they will be taken into consideration in the secondary analyses of neonatal outcomes.

Sites / Locations

  • Cameroon Baptist Convention Health Services

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Placebo Comparator

Arm Label

Azithromycin and amoxicillin placebo

Azithromycin + amoxicillin

Usual Care

Arm Description

Patients in this arm will receive 1 gram oral azithromycin as a single dose and amoxicillin placebo.

Patients in this arm will receive 1 gram oral azithromycin and 2 grams oral amoxicillin in a single dose.

This arm will consist of routine care at the clinical sites (which is usually no antibiotic). They will receive placebo (for azithromycin) and placebo (for amoxicillin)

Outcomes

Primary Outcome Measures

Number of Participants Who Experienced Composite Peripartum Infection or Death
Maternal peripartum infection including chorioamnionitis, endometritis, wound infection/abscess, sepsis, and death

Secondary Outcome Measures

Number of Participants Who Experienced Pyelonephritis
Other Infections
Number of Participants Who Experienced Breast Infection
Other infections
Number of Participants Who Experienced Other Infection
Includes Hepatitis B, thyroid infection, vaginal infection, viral infection, leg cellulitis, unknown abdominal infection,malaria
Number of Participants Who Experienced Fever
Any fever higher than 38C
Number of Participants Who Experienced Hypothermia
Any hypothermia less than 36C
Number of Participants Who Needed PP Antibiotic
Any postpartum antibiotic
Number of Participants Who Experienced Transfusion
Blood transfusion
Number of Participants Who Experienced Stillbirth
Any stillbirth
Length of Stay
Length of stay in days
Number of Participants Who Experienced a Clinic Visit
Clinic visit after discharge
Number of Participants Who Experienced a Maternal Readmission
Maternal readmission

Full Information

First Posted
July 25, 2017
Last Updated
March 18, 2022
Sponsor
University of Alabama at Birmingham
Collaborators
Merck Sharp & Dohme LLC
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1. Study Identification

Unique Protocol Identification Number
NCT03248297
Brief Title
Antibiotic Prophlaxis for High-risk Laboring Women in Low Income Countries
Official Title
Azithromycin With or Without Amoxicillin to Prevent Peripartum Infection and Sepsis in Laboring High-risk Women: 3-Arm RCT
Study Type
Interventional

2. Study Status

Record Verification Date
March 2022
Overall Recruitment Status
Completed
Study Start Date
January 12, 2018 (Actual)
Primary Completion Date
May 15, 2020 (Actual)
Study Completion Date
October 1, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Alabama at Birmingham
Collaborators
Merck Sharp & Dohme LLC

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
This study, performed over a course of 3 years in 5 collaborating hospitals in Cameroon, Africa, will randomize 750 women in labor with prolonged rupture of membranes ≥ 8 hours or prolonged labor ≥ 18 hours to identical oral regimens of 1 gram of azithromycin, 1 gram of azithromycin+2 grams of amoxicillin or placebo. Women will be followed to ascertain maternal infectious outcomes and perinatal outcomes.
Detailed Description
This 3-arm study is a large randomized clinical trial designed to evaluate the comparative effectiveness and safety of single dose oral azithromycin or combined azithromycin+amoxicillin compared to placebo for the prevention of peripartum infections and sepsis in laboring women. We have previously shown the effectiveness of azithromycin for extended spectrum antibiotic prophylaxis in addition to the standard cephalosporin alone for reduction of post-cesarean infections. In LICs, the fraction of maternal infection and sepsis from cesarean delivery is minimal. Therefore, it is necessary to evaluate strategies aimed at reducing these morbidities in women who have vaginal births. There is an increased risk of infection in women who have prolonged labor or prolonged rupture of membranes. Drawing from our findings with azithromycin-based extended antibiotic prophylaxis for cesarean delivery, we propose to adapt the intervention and evaluate a single oral dose of azithromycin (with or without oral amoxicillin) to prevent maternal peripartum infection and sepsis. This study, performed over a course of 3 years in 5 collaborating hospitals in Cameroon, Africa, will randomize 750 women in labor with prolonged rupture of membranes ≥ 8 hours or prolonged labor ≥18 hours to 1 gram of oral azithromycin, 1 gram of azithromycin+2 grams of amoxicillin, compared to usual care (placebo). Women will be followed to ascertain maternal infectious outcomes and perinatal outcomes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Postpartum Sepsis, Postpartum Endometritis, Postpartum Fever

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Randomized Controlled Trial
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
756 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Azithromycin and amoxicillin placebo
Arm Type
Experimental
Arm Description
Patients in this arm will receive 1 gram oral azithromycin as a single dose and amoxicillin placebo.
Arm Title
Azithromycin + amoxicillin
Arm Type
Experimental
Arm Description
Patients in this arm will receive 1 gram oral azithromycin and 2 grams oral amoxicillin in a single dose.
Arm Title
Usual Care
Arm Type
Placebo Comparator
Arm Description
This arm will consist of routine care at the clinical sites (which is usually no antibiotic). They will receive placebo (for azithromycin) and placebo (for amoxicillin)
Intervention Type
Drug
Intervention Name(s)
Azithromycin
Intervention Description
Azithromycin tablet
Intervention Type
Drug
Intervention Name(s)
Azithromycin and amoxicillin
Other Intervention Name(s)
azithromycin, amoxicillin
Intervention Description
azithromycin and amoxicillin
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo tablet
Primary Outcome Measure Information:
Title
Number of Participants Who Experienced Composite Peripartum Infection or Death
Description
Maternal peripartum infection including chorioamnionitis, endometritis, wound infection/abscess, sepsis, and death
Time Frame
Up to 6 weeks after delivery
Secondary Outcome Measure Information:
Title
Number of Participants Who Experienced Pyelonephritis
Description
Other Infections
Time Frame
Up to hospital discharge
Title
Number of Participants Who Experienced Breast Infection
Description
Other infections
Time Frame
Up to 6 weeks after delivery
Title
Number of Participants Who Experienced Other Infection
Description
Includes Hepatitis B, thyroid infection, vaginal infection, viral infection, leg cellulitis, unknown abdominal infection,malaria
Time Frame
up to 6 weeks after delivery
Title
Number of Participants Who Experienced Fever
Description
Any fever higher than 38C
Time Frame
up to 6 weeks after delivery
Title
Number of Participants Who Experienced Hypothermia
Description
Any hypothermia less than 36C
Time Frame
up to 6 weeks after delivery
Title
Number of Participants Who Needed PP Antibiotic
Description
Any postpartum antibiotic
Time Frame
up to 6 weeks after delivery
Title
Number of Participants Who Experienced Transfusion
Description
Blood transfusion
Time Frame
up to 6 weeks after delivery
Title
Number of Participants Who Experienced Stillbirth
Description
Any stillbirth
Time Frame
delivery
Title
Length of Stay
Description
Length of stay in days
Time Frame
up to 6 weeks postpartum
Title
Number of Participants Who Experienced a Clinic Visit
Description
Clinic visit after discharge
Time Frame
up to 6 weeks after delivery
Title
Number of Participants Who Experienced a Maternal Readmission
Description
Maternal readmission
Time Frame
up to 6 weeks after delivery

10. Eligibility

Sex
Female
Gender Based
Yes
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Women ≥ 37 weeks' viable singleton or twin gestation in labor planning a vaginal delivery with Prolonged membrane rupture (≥8 hours) or Prolonged labor (≥18 hours). Exclusion Criteria: Clinical chorioamnionitis or any other active bacterial infection (e.g. pyelonephritis, pneumonia, abscess) at time of randomization: because standard antibiotic therapy for these conditions may confound trial intervention. Allergy to azithromycin or amoxicillin Plan for cesarean delivery prior to enrollment Fetal demise or major congenital anomaly: Major congenital anomalies may confound assessment of neonatal outcomes and every attempt will be made up front to exclude them from randomization. However, some unrecognized fetal anomalies may inevitably be randomized. These will not be excluded post-randomization from the primary (maternal outcome) analysis; they will be taken into consideration in the secondary analyses of neonatal outcomes.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alan Tita, MD, PhD
Organizational Affiliation
University of Alabama at Birmingham
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cameroon Baptist Convention Health Services
City
Bamenda
Country
Cameroon

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
10196487
Citation
Mangram AJ, Horan TC, Pearson ML, Silver LC, Jarvis WR. Guideline for Prevention of Surgical Site Infection, 1999. Centers for Disease Control and Prevention (CDC) Hospital Infection Control Practices Advisory Committee. Am J Infect Control. 1999 Apr;27(2):97-132; quiz 133-4; discussion 96.
Results Reference
background
PubMed Identifier
10511234
Citation
ASHP Therapeutic Guidelines on Antimicrobial Prophylaxis in Surgery. American Society of Health-System Pharmacists. Am J Health Syst Pharm. 1999 Sep 15;56(18):1839-88. doi: 10.1093/ajhp/56.18.1839. No abstract available.
Results Reference
background
PubMed Identifier
28076707
Citation
Tita ATN, Boggess K, Saade G. Adjunctive Azithromycin Prophylaxis for Cesarean Delivery. N Engl J Med. 2017 Jan 12;376(2):182. doi: 10.1056/NEJMc1614626. No abstract available.
Results Reference
background
Citation
WHO. WHO recommendations for prevention and treatment of maternal peripartum infections. Sept 2015 http://www.who.int/reproductivehealth/publications/maternal_perinatal_health/peripartum-infections-guidelines/en/
Results Reference
background
PubMed Identifier
34619734
Citation
Subramaniam A, Ye Y, Mbah R, Mbunwe DM, Pekwarake S, Bunwi EY, Fondzeyuf A, Ngong MG, Dionne-Odom J, Harper LM, Jauk VC, Carlo WA, Halle-Ekane G, Szychowski JM, Tih P, Tita AT. Single Dose of Oral Azithromycin With or Without Amoxicillin to Prevent Peripartum Infection in Laboring, High-Risk Women in Cameroon: A Randomized Controlled Trial. Obstet Gynecol. 2021 Nov 1;138(5):703-713. doi: 10.1097/AOG.0000000000004565.
Results Reference
derived

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Antibiotic Prophlaxis for High-risk Laboring Women in Low Income Countries

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