- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01232192
Study of Antenatal Model to Prevent Preterm Delivery (AACP)
November 1, 2010 updated by: Showa University
Study of Antenatal Model to Prevent Preterm Delivery: Early Detection and Treatment of Bacterial Vaginosis
The purpose of this study is to determine whether antenatal model in vaginosis are effective in preventing vaginal infection and preterm delivery
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
The standard antenatal care nowadays can not answer for preterm delivery problems.
Thus, comprehensive and proactive approach is needed for preventing preterm delivery.
This antenatal model is consisted of midwife training, early detection of bacterial vaginosis, pregnant women campaign and self administered pH check
Study Type
Interventional
Enrollment (Anticipated)
220
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Jakarta, Indonesia, 13210
- Recruiting
- Cipto Mangunkusumo National Hospital
-
Contact:
- Ali Sungkar, MD, PhD
- Email: alisungkar@yahoo.com
-
Contact:
- Yuditiya Purwosunu, MD
- Email: yudi@med.showa-u.ac.jp
-
Principal Investigator:
- Ali Sungkar, MD, PhD
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years to 40 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- 14- 18 week gestation pregnant women with or without any vaginal discharge
- singleton pregnancy, without any fetal or uterine anomaly
Exclusion Criteria:
- Any complication in pregnancy
- Any history of disease in pregnancy
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Antenatal model
|
Antenatal model is consisted of integrated efforts to lower preterm delivery rate through early detection and bacterial vaginal infection treatment:
Other Names:
|
|
Experimental: Antenatal Model
|
Antenatal model is consisted of integrated efforts to lower preterm delivery rate through early detection and bacterial vaginal infection treatment:
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
all preterm delivery
Time Frame: 37 weeks
|
37 weeks
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
knowledge of midwife about preterm
Time Frame: one year
|
one year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Ali Sungkar, MD, PhD, Dept Obstetrics Gynecology, Indonesia University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2009
Primary Completion (Anticipated)
January 1, 2011
Study Completion (Anticipated)
March 1, 2011
Study Registration Dates
First Submitted
November 1, 2010
First Submitted That Met QC Criteria
November 1, 2010
First Posted (Estimate)
November 2, 2010
Study Record Updates
Last Update Posted (Estimate)
November 2, 2010
Last Update Submitted That Met QC Criteria
November 1, 2010
Last Verified
March 1, 2009
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- AACP09
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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