- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05513768
PRETERM DELİVERY and MYOCINE BINDING PROTEIN C LEVELs
Can First Trimester Serum Myocine Binding Protein c Level Predict Preterm Birth
IT WAS AIMED TO EVALUATE IF MBPC CAN BE USED IN PREDICTION OF EARLY BIRTH. TAKING THE FIRST TRIMESTER FROM PREGNANCY WAS STORED UNTIL THE TIMING OF DELIVERY.THE PARTICIPANTS WERE SEPARATED INTO TWO GROUPS ACCORDING TO THE TIME OF BIRTH, EARLY AND TIMELY.
SERUM MBPC LEVELS BETWEEN TWO GROUPS EVALUATED.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
IT WAS AIMED TO EVALUATE IF MBPC CAN BE USED IN PREDICTION OF EARLY BIRTH. TAKING THE FIRST TRIMESTER FROM PREGNANCY WAS STORED UNTIL THE TIMING OF DELIVERY.THE PARTICIPANTS WERE SEPARATED INTO TWO GROUPS ACCORDING TO THE TIME OF BIRTH, EARLY AND TIMELY.
SERUM MBPC LEVELS BETWEEN TWO GROUPS EVALUATED.A TOTAL OF 90 WOMEN WERE PLANNED TO INCLUDE 45 STUDY 45 CONTROL GROUP IN THE STUDY.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Gaziosmanpaşa
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Istanbul, Gaziosmanpaşa, Turkey, 32225
- Gaziosmanpasa Training and Research Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- being pregnant in the first trimester
- be between 18-40 years old
Exclusion Criteria:
- no history of preterm birth
- being pregnant with assisted reproductive techniques
- having a multiple pregnancy
- have cervical insufficiency
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
women who gave birth prematurely
women who had serum taken in the first trimester and gave birth earlier than 37 weeks according to the time of delivery
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Serum samples will be taken from the participants in the first trimester, transferred to eppendorf tubes after appropriate procedures, and stored at -80 degrees until the time of deliveryParticipants will be divided into two groups according to the timing of birthThe first group is those who gave birth earlier than 37 weeks those who gave birth on time in the other group The mbpc levels will be looked at and compared.
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those who gave birth on time
women who have had serum taken in the first trimester, stored and delivered on time
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Serum samples will be taken from the participants in the first trimester, transferred to eppendorf tubes after appropriate procedures, and stored at -80 degrees until the time of deliveryParticipants will be divided into two groups according to the timing of birthThe first group is those who gave birth earlier than 37 weeks those who gave birth on time in the other group The mbpc levels will be looked at and compared.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
detection of prediction value of serum mbpc levels in preterm delivery
Time Frame: 10 mounths
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identifying prediction value of first trmester serum mbpc levels by comparing by serum levels of mbpc in groups
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10 mounths
|
Collaborators and Investigators
Investigators
- Principal Investigator: elif yıldız, Gaziosmanpasa Research and Education Hospital
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- GaziosmanpasaTREHKHD
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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