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Revealed Versus Concealed Cerebroplacental Ratio

Primary Purpose

Stillbirth

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Revealment
Sponsored by
Hospital Clinic of Barcelona
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Stillbirth focused on measuring stillbirth, cerebroplacental ratio, fetal growth restriction

Eligibility Criteria

18 Years - 50 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Viable singleton non-malformed fetus
  • Available first-trimester US dating
  • Maternal age at recruitment ≥18 years
  • No adverse medical or obstetrical history at booking
  • Capacity to give informed consent

Exclusion Criteria:

  • Abnormal karyotype
  • Structural abnormalities
  • Congenital infections

Sites / Locations

  • Hospital Clínico Universitario de Santiago de Chile
  • Palacky University Hospital
  • Ladislav Krofta
  • Eyal Zohav
  • Hospital de Querétaro
  • Anna Kajdy
  • Hospital Clinic
  • Elena Escazzocchio
  • Elena Ferriols Perez

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Other

Arm Label

Concealment

Revealment

Arm Description

Cerebroplacental ratio measurement at 37 weeks of pregnancy only taken into account if estimated fetal weight <p10

Cerebroplacental ratio measurement at 37weeks and labor induction in case of cerebroplacental ratio <p5

Outcomes

Primary Outcome Measures

Stillbirth
Perinatal death

Secondary Outcome Measures

Adverse perinatal outcome
Severe neurological and non-neurological adverse outcome
Fetal Growth Restriction Detection
To detect prenatal low birth weight

Full Information

First Posted
August 1, 2016
Last Updated
April 11, 2022
Sponsor
Hospital Clinic of Barcelona
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1. Study Identification

Unique Protocol Identification Number
NCT02907242
Brief Title
Revealed Versus Concealed Cerebroplacental Ratio
Official Title
Revealed Versus Concealed Criteria for Placental Insufficiency in Unselected Obstetric Population in Late Pregnancy: a Multicenter Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Completed
Study Start Date
May 4, 2016 (Actual)
Primary Completion Date
January 6, 2022 (Actual)
Study Completion Date
January 6, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital Clinic of Barcelona

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to evaluate the role of an integrated strategy at selecting fetuses for delivery at term based on a combination of fetal biometry and cerebroplacental ratio (CPR) to reduce stillbirth rate and adverse perinatal outcome.
Detailed Description
This is a multicenter, open-label randomized trial with groups in parallel. Singleton pregnancies are recruited after routine second trimester scan (19+0 to 22+6 weeks of gestation) and randomly allocated at that moment to revealed or concealed strategy. A routine scan will be booked at 36-37 weeks. For a reduction of the stillbirth rate of 3‰ (from 5‰ to 2‰), assuming a type I error of 5% and aiming for a power of 80% a total of 11,582 subjects (5791 per arm) were projected. The participating centers sum up 12,000 deliveries a year. It is not possible to blind participants, obstetricians, or outcome assessors to the study group. General hypothesis: A proportion of fetuses with "normal" growth as per current standards have placental insufficiency and restriction of their growth potential. These fetuses exhibit biophysical changes expressed by abnormal cerebroplacental ratio. A combination of this marker with fetal biometry for the detection of fetuses affected by fetal growth restriction could identify a group of babies on which labor induction once term is reached may prevent the occurrence of adverse outcomes. Specific hypothesis The cerebroplacental ratio has predictive value in late pregnancy for placental insufficiency. The cerebroplacental ratio could improve the effectiveness of late pregnancy screening for the prediction placental insufficiency-related complications.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stillbirth
Keywords
stillbirth, cerebroplacental ratio, fetal growth restriction

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
11582 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Concealment
Arm Type
No Intervention
Arm Description
Cerebroplacental ratio measurement at 37 weeks of pregnancy only taken into account if estimated fetal weight <p10
Arm Title
Revealment
Arm Type
Other
Arm Description
Cerebroplacental ratio measurement at 37weeks and labor induction in case of cerebroplacental ratio <p5
Intervention Type
Other
Intervention Name(s)
Revealment
Intervention Description
Cerebroplacental ratio revealment
Primary Outcome Measure Information:
Title
Stillbirth
Description
Perinatal death
Time Frame
between 37 and 42 weeks of pregnancy
Secondary Outcome Measure Information:
Title
Adverse perinatal outcome
Description
Severe neurological and non-neurological adverse outcome
Time Frame
Up to 28 days after delivery
Title
Fetal Growth Restriction Detection
Description
To detect prenatal low birth weight
Time Frame
3 years

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Viable singleton non-malformed fetus Available first-trimester US dating Maternal age at recruitment ≥18 years No adverse medical or obstetrical history at booking Capacity to give informed consent Exclusion Criteria: Abnormal karyotype Structural abnormalities Congenital infections
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Eduard Gratacos, PhD
Organizational Affiliation
Hospital Clinic
Official's Role
Study Chair
Facility Information:
Facility Name
Hospital Clínico Universitario de Santiago de Chile
City
Santiago de Chile
Country
Chile
Facility Name
Palacky University Hospital
City
Olomouc
Country
Czechia
Facility Name
Ladislav Krofta
City
Prague
Country
Czechia
Facility Name
Eyal Zohav
City
Tel Aviv
Country
Israel
Facility Name
Hospital de Querétaro
City
Querétaro
Country
Mexico
Facility Name
Anna Kajdy
City
Warsaw
Country
Poland
Facility Name
Hospital Clinic
City
Barcelona
ZIP/Postal Code
08036
Country
Spain
Facility Name
Elena Escazzocchio
City
Barcelona
Country
Spain
Facility Name
Elena Ferriols Perez
City
Barcelona
Country
Spain

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
28619771
Citation
Figueras F, Gratacos E, Rial M, Gull I, Krofta L, Lubusky M, Cruz-Martinez R, Cruz-Lemini M, Martinez-Rodriguez M, Socias P, Aleuanlli C, Cordero MCP. Revealed versus concealed criteria for placental insufficiency in an unselected obstetric population in late pregnancy (RATIO37): randomised controlled trial study protocol. BMJ Open. 2017 Jun 15;7(6):e014835. doi: 10.1136/bmjopen-2016-014835. Erratum In: BMJ Open. 2019 Feb 19;9(2):e014835corr1.
Results Reference
derived

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Revealed Versus Concealed Cerebroplacental Ratio

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