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Chlorhexidine Vaginal and Infant Wash in Pakistan

Primary Purpose

Sepsis, Pregnancy

Status
Completed
Phase
Phase 3
Locations
Pakistan
Study Type
Interventional
Intervention
Chlorhexidine vaginal and infant wash
Sponsored by
NICHD Global Network for Women's and Children's Health
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Sepsis focused on measuring Chlorhexidine, Vaginal wash, Neonatal mortality, Sepsis, Global Network, Maternal and child health, Women's Health, International, Pakistan

Eligibility Criteria

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

Inclusion Criteria: Gravidas with living fetus delivering at home in the care of identified study birth attendant (community) or admitted to the identified hospital (Civil Hospital Karachi) for delivery Exclusion Criteria: Contraindications to cervical exam (e.g., placenta previa) Active genital herpes or vulvovaginal ulceration Known or suspected allergy to chlorhexidine Fetus with face presentation Fetal death Unwilling/unable to give informed consent Less than 16 years of age

Sites / Locations

  • Civil Hospital Karachi

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Chlorhexidine

Arm Description

Outcomes

Primary Outcome Measures

Neonatal death or severe sepsis

Secondary Outcome Measures

Maternal: clinical chorioamnionitis, clinical endometritis, urinary tract infection, sepsis, length of hospitalization, readmission to hospital, death
Neonatal: receipt of antibiotics, duration of hospitalization, readmission to hospital

Full Information

First Posted
July 15, 2005
Last Updated
July 29, 2014
Sponsor
NICHD Global Network for Women's and Children's Health
Collaborators
Global Network for Women's and Children's Health Research, Bill and Melinda Gates Foundation, RTI International, University of Alabama at Birmingham, Aga Khan University, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
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1. Study Identification

Unique Protocol Identification Number
NCT00121394
Brief Title
Chlorhexidine Vaginal and Infant Wash in Pakistan
Official Title
Randomized Trial of Chlorhexidine Vaginal and Infant Wash to Reduce Neonatal Mortality
Study Type
Interventional

2. Study Status

Record Verification Date
July 2014
Overall Recruitment Status
Completed
Study Start Date
June 2005 (undefined)
Primary Completion Date
June 2008 (Actual)
Study Completion Date
June 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
NICHD Global Network for Women's and Children's Health
Collaborators
Global Network for Women's and Children's Health Research, Bill and Melinda Gates Foundation, RTI International, University of Alabama at Birmingham, Aga Khan University, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Infection is a major health problem during birth in Pakistan. This study will look at the possibility of using a septic wash to help improve health during birth in Karachi, Pakistan.
Detailed Description
Sepsis in mother and infant is a major cause of perinatal morbidity and mortality in low-resource settings. Several studies have investigated the likelihood that an anti-bacterial agent, chlorhexidine, administered during labor and delivery to mother and infant could reduce the risk of infection and of subsequent maternal and infant morbidity and mortality. In this trial, chlorhexidine wash and placebo will be randomly administered to women in labor and newborn infants in a public hospital in Karachi, Pakistan. Delivery attendants will administer 0.6% chlorhexidine solution every four hours until delivery (4 washes maximum) and one neonatal wash with the same solution. The control group will receive 200 ml of sterile physiologic saline solution. A total of 5000 women will be randomized in the hospital study, 2500 control and 2500 intervention. All women and infants will be evaluated 24 hours post delivery and at a 7-day follow-up. Women who delivered at home will also receive a 28 days post-partum assessment. Women will be carefully monitored for side effects to the dosage. In addition a community-based feasibility trial of 200 patients (100 CHX, 100 control) will be completed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sepsis, Pregnancy
Keywords
Chlorhexidine, Vaginal wash, Neonatal mortality, Sepsis, Global Network, Maternal and child health, Women's Health, International, Pakistan

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
5008 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Chlorhexidine
Arm Type
Experimental
Intervention Type
Procedure
Intervention Name(s)
Chlorhexidine vaginal and infant wash
Primary Outcome Measure Information:
Title
Neonatal death or severe sepsis
Time Frame
7 days
Secondary Outcome Measure Information:
Title
Maternal: clinical chorioamnionitis, clinical endometritis, urinary tract infection, sepsis, length of hospitalization, readmission to hospital, death
Time Frame
7 days
Title
Neonatal: receipt of antibiotics, duration of hospitalization, readmission to hospital
Time Frame
7 dats

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Gravidas with living fetus delivering at home in the care of identified study birth attendant (community) or admitted to the identified hospital (Civil Hospital Karachi) for delivery Exclusion Criteria: Contraindications to cervical exam (e.g., placenta previa) Active genital herpes or vulvovaginal ulceration Known or suspected allergy to chlorhexidine Fetus with face presentation Fetal death Unwilling/unable to give informed consent Less than 16 years of age
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robert Goldenberg, M.D.
Organizational Affiliation
Drexel University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Sarah Saleem, M.D.
Organizational Affiliation
The Aga Khan University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Civil Hospital Karachi
City
Karachi
Country
Pakistan

12. IPD Sharing Statement

Citations:
PubMed Identifier
20502294
Citation
Saleem S, Rouse DJ, McClure EM, Zaidi A, Reza T, Yahya Y, Memon IA, Khan NH, Memon G, Soomro N, Pasha O, Wright LL, Moore J, Goldenberg RL. Chlorhexidine vaginal and infant wipes to reduce perinatal mortality and morbidity: a randomized controlled trial. Obstet Gynecol. 2010 Jun;115(6):1225-1232. doi: 10.1097/AOG.0b013e3181e00ff0.
Results Reference
derived
PubMed Identifier
17978107
Citation
Saleem S, Reza T, McClure EM, Pasha O, Moss N, Rouse DJ, Bartz J, Goldenberg RL. Chlorhexidine vaginal and neonatal wipes in home births in Pakistan: a randomized controlled trial. Obstet Gynecol. 2007 Nov;110(5):977-85. doi: 10.1097/01.AOG.0000285653.17869.26.
Results Reference
derived
Links:
URL
http://gn.rti.org
Description
Global Network for Women's and Children's Health Research
URL
http://www.rti.org/
Description
Research Triangle Institute International
URL
http://www.aku.edu/
Description
Aga Khan University, Pakistan

Learn more about this trial

Chlorhexidine Vaginal and Infant Wash in Pakistan

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