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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05513768
Other study ID # GaziosmanpasaTREHKHD
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2022
Est. completion date October 30, 2022

Study information

Verified date November 2022
Source Gaziosmanpasa Research and Education Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 90
Est. completion date October 30, 2022
Est. primary completion date October 30, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 40 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
level of myosin binding protein c in serum
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.

Locations

Country Name City State
Turkey Gaziosmanpasa Training and Research Hospital Istanbul Gaziosmanpasa

Sponsors (1)

Lead Sponsor Collaborator
Gaziosmanpasa Research and Education Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary detection of prediction value of serum mbpc levels in preterm delivery identifying prediction value of first trmester serum mbpc levels by comparing by serum levels of mbpc in groups 10 mounths
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