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Management of Fetal Growth Restriction at Term: Angiogenic Factors Versus Feto-placental Doppler (GRAFD)

Primary Purpose

Fetal Growth Retardation

Status
Unknown status
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Management based on sFlt-1/PlGF values
Sponsored by
Hospital Universitari Vall d'Hebron Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fetal Growth Retardation

Eligibility Criteria

16 Years - undefined (Child, Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  1. Pregnant women ≥ 16 years of age.
  2. Singleton pregnancy.
  3. Ultrasonographic estimated fetal weight <10th centile.
  4. Gestational age between 36+0 and 37+6 weeks.

Exclusion Criteria:

  1. Major fetal malformations or genetic disorders.
  2. Fetal death.
  3. Absent or reverse end-diastolic flow in umbilical artery Doppler or DV PI>95th centile.
  4. Non-reassuring cardiotocography (CTG).
  5. Preeclampsia.
  6. Diminished fetal movements.
  7. Biophysical profile ≤ 6.
  8. Oligohydramnios
  9. Refusal to give informed consent.

Sites / Locations

  • Hospital Universitario de A CoruñaRecruiting
  • Hospital General de AlicanteRecruiting
  • Hospital Germans Trias i PujolRecruiting
  • Hospital Universitari Vall d'hebronRecruiting
  • Hospital Universitario de CabueñesRecruiting
  • Hospital Universitario Puerta del MarRecruiting
  • Hospital General Universitario de ElcheRecruiting
  • Hospital Universitario de GetafeRecruiting
  • Hospital Universitari Doctor Josep TruetaRecruiting
  • Hospital Sant Joan de Deu de ManresaRecruiting
  • Hospital Clínico Universitario Virgen de la ArrixacaRecruiting
  • Hospital Son LlàtzerRecruiting
  • Consorci Corporació Sanitària Parc Taulí de SabadellRecruiting
  • Hospital Universitario Nuestra Señora de CandelariaRecruiting
  • Hospital Universitario Virgen de ValmeRecruiting
  • Hospital Universitari Joan XXIIIRecruiting
  • Hospital de TerrassaRecruiting
  • Hospital Universitari Mútua TerrassaRecruiting
  • Hospital Universitario de TorrejonRecruiting
  • Hospital Clinico Universitario Lozano BlesaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Control Group

Intervention Group

Arm Description

Clinical practice: Management by Doppler and CTG findings. In women allocated to the control group, the sFlt-1/PlGF result will be blinded to caregivers. Routine Doppler-based clinical care will be used to counsel women. Following the Doppler classification: Fetuses with an EFW below the 3rd centile or below the 10th centile accompanied by any impaired fetoplacental Doppler, elective delivery will be recommended immediately (within 24h) at ≥37 weeks. Fetuses with an EFW above the 3rd centile without any fetoplacental Doppler abnormality, elective delivery will be recommended at at ≥40 weeks.

Management based on sFlt-1/PlGF values

Outcomes

Primary Outcome Measures

Adverse perinatal outcomes
Cesarean delivery for non-reassuring fetal status or neonatal acidosis (artery cord potential of hydrogen (pH) <7.15 + base excess > -12 milliequivalent/L)

Secondary Outcome Measures

Rate of elective delivery
Percentage of women that required an elective delivery
Rate of Cesarean delivery
Percentage of women that required a Cesarean delivery
Rate of Induction of labor
Percentage of women that required an induction of labor
Rate of neonatal admission in intensive care unit
Percentage of newborns that required admission in intensive care
Time of neonatal admission in intensive care unit
Days in in intensive care of newborns that required admission
Rate of preeclampsia
Percentage of women that developed preeclampsia
Rate of neonatal complications
Percentage of newborns with adverse outcomes (composite)
Rate of maternal complications
Percentage of women with adverse outcomes (composite)
Rate of perinatal complications
Percentage of perinatal adverse outcomes (composite)
Rate of total deliveries at <37, <38, <39 and <40 weeks of gestation
Percentage of women that delivered at <37, <38, <39 and <40 weeks of gestation
Rate of elective deliveries at <37, <38, <39 and <40 weeks of gestation
Percentage of women that delivered electively at <37, <38, <39 and <40 weeks of gestation
Rate of newborns with birthweight <2000 and <2500 grams
Percentage of women that delivered a newborn with a birthweight <2000 and <2500 grams

Full Information

First Posted
August 4, 2020
Last Updated
December 20, 2021
Sponsor
Hospital Universitari Vall d'Hebron Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT04502823
Brief Title
Management of Fetal Growth Restriction at Term: Angiogenic Factors Versus Feto-placental Doppler
Acronym
GRAFD
Official Title
Management of Fetal Growth Restriction at Term: Angiogenic Factors Versus Feto-placental Doppler (GRAFD Trial)
Study Type
Interventional

2. Study Status

Record Verification Date
July 2021
Overall Recruitment Status
Unknown status
Study Start Date
September 21, 2020 (Actual)
Primary Completion Date
December 31, 2022 (Anticipated)
Study Completion Date
December 31, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospital Universitari Vall d'Hebron Research Institute

4. Oversight

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

5. Study Description

Brief Summary
Open randomized non-inferiority controlled trial to examine the use of angiogenic factors (instead of feto-placental Doppler) for fetal growth restriction at term to reduce the rate of labor inductions, without worsening perinatal outcomes.
Detailed Description
Pregnant women with estimated fetal weight (EFW) < 10th centile between 36+0 and 37+6 weeks of gestation (WG) will receive complete ultrasonographic assessment consisting of feto-placental Doppler, amniotic fluid measurement and biophysical profile assessment. The cases not meeting any exclusion criteria will be offered to participate in this trial. After giving their informed consent a blood sample will be drawn in all of them and they will undergo randomization into two arms. Intervention arm: In women allocated to the intervention group, the soluble fms-like tyrosine kinase/placental growth factor (sFlt-1/PlGF) result will be revealed to the investigators that will act according to the results of sFlt/PlGF: Fetuses with sFlt-1/PlGF ≥38, elective delivery will be recommended at ≥37 weeks. Fetuses with sFlt-1/PlGF <38, weekly follow up will be recommended until delivery (at ≥40 weeks). Control arm: In women allocated to the control group, the sFlt-1/PlGF result will be blinded to caregivers. Routine Doppler-based clinical care will be used to counsel women. Following the Doppler classification: Fetuses with EFW below the 3rd centile or below the 10th centile accompanied by any impaired fetoplacental Doppler, elective delivery will be recommended at at ≥37 weeks. Fetuses with EFW above the 3rd centile without any fetoplacental Doppler abnormality, elective delivery will be recommended at at ≥40 weeks. In both arms, fetuses will receive weekly follow-up from randomization to delivery consisting on feto-placental Doppler sFlt-1/PlGF and CTG. If any of the following is present at any time, earlier delivery will be recommended: sFlt-1/PlGF ≥38 (only in the intervention group), absent or reverse end-diastolic flow at the umbilical artery Doppler or DV PI>95th centile non-reassuring CTG preeclampsia diminished fetal movements biophysical profile ≤ 6 or oligohydramnios (deepest pocket <2 cm).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fetal Growth Retardation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1030 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Control Group
Arm Type
No Intervention
Arm Description
Clinical practice: Management by Doppler and CTG findings. In women allocated to the control group, the sFlt-1/PlGF result will be blinded to caregivers. Routine Doppler-based clinical care will be used to counsel women. Following the Doppler classification: Fetuses with an EFW below the 3rd centile or below the 10th centile accompanied by any impaired fetoplacental Doppler, elective delivery will be recommended immediately (within 24h) at ≥37 weeks. Fetuses with an EFW above the 3rd centile without any fetoplacental Doppler abnormality, elective delivery will be recommended at at ≥40 weeks.
Arm Title
Intervention Group
Arm Type
Experimental
Arm Description
Management based on sFlt-1/PlGF values
Intervention Type
Procedure
Intervention Name(s)
Management based on sFlt-1/PlGF values
Intervention Description
In women allocated to the intervention group, the sFlt-1/PlGF result will be revealed to the investigators that will act according to the results of sFlt/PlGF: Fetuses with sFlt-1/PlGF ≥38, elective delivery will be recommended immediately (within 24h) at ≥37 weeks. Fetuses with sFlt-1/PlGF <38 weekly follow up will be recommended and delivery at ≥40 weeks.
Primary Outcome Measure Information:
Title
Adverse perinatal outcomes
Description
Cesarean delivery for non-reassuring fetal status or neonatal acidosis (artery cord potential of hydrogen (pH) <7.15 + base excess > -12 milliequivalent/L)
Time Frame
4-6 weeks
Secondary Outcome Measure Information:
Title
Rate of elective delivery
Description
Percentage of women that required an elective delivery
Time Frame
4-6 weeks
Title
Rate of Cesarean delivery
Description
Percentage of women that required a Cesarean delivery
Time Frame
4-6 weeks
Title
Rate of Induction of labor
Description
Percentage of women that required an induction of labor
Time Frame
4-6 weeks
Title
Rate of neonatal admission in intensive care unit
Description
Percentage of newborns that required admission in intensive care
Time Frame
4-6 weeks
Title
Time of neonatal admission in intensive care unit
Description
Days in in intensive care of newborns that required admission
Time Frame
4-6 weeks
Title
Rate of preeclampsia
Description
Percentage of women that developed preeclampsia
Time Frame
4-6 weeks
Title
Rate of neonatal complications
Description
Percentage of newborns with adverse outcomes (composite)
Time Frame
4-10 weeks
Title
Rate of maternal complications
Description
Percentage of women with adverse outcomes (composite)
Time Frame
4-6 weeks
Title
Rate of perinatal complications
Description
Percentage of perinatal adverse outcomes (composite)
Time Frame
4-6 weeks
Title
Rate of total deliveries at <37, <38, <39 and <40 weeks of gestation
Description
Percentage of women that delivered at <37, <38, <39 and <40 weeks of gestation
Time Frame
4-6 weeks
Title
Rate of elective deliveries at <37, <38, <39 and <40 weeks of gestation
Description
Percentage of women that delivered electively at <37, <38, <39 and <40 weeks of gestation
Time Frame
4-6 weeks
Title
Rate of newborns with birthweight <2000 and <2500 grams
Description
Percentage of women that delivered a newborn with a birthweight <2000 and <2500 grams
Time Frame
4-6 weeks

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
pregnant women
Minimum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Pregnant women ≥ 16 years of age. Singleton pregnancy. Ultrasonographic estimated fetal weight <10th centile. Gestational age between 36+0 and 37+6 weeks. Exclusion Criteria: Major fetal malformations or genetic disorders. Fetal death. Absent or reverse end-diastolic flow in umbilical artery Doppler or DV PI>95th centile. Non-reassuring cardiotocography (CTG). Preeclampsia. Diminished fetal movements. Biophysical profile ≤ 6. Oligohydramnios Refusal to give informed consent.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Manel Mendoza, PhD
Phone
0034934893000
Ext
3085
Email
mmendoza@vhebron.net
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Manel Mendoza, PhD
Organizational Affiliation
Vall d'hebron Institut de Recerca
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Universitario de A Coruña
City
A Coruña
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nuria Valiño
Email
nuvalino@gmail.com
Facility Name
Hospital General de Alicante
City
Alicante
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ana Palacios
Email
ana.palacios.marques@gmail.com
Facility Name
Hospital Germans Trias i Pujol
City
Badalona
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ivan Hurtado
Email
ivan.hurtado85@gmail.com
Facility Name
Hospital Universitari Vall d'hebron
City
Barcelona
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Manel Mendoza
Email
mmendoza@vhebron.net
Facility Name
Hospital Universitario de Cabueñes
City
Cabueñes
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Esther Perez
Email
estherpcarbajo@hotmail.com
Facility Name
Hospital Universitario Puerta del Mar
City
Cadiz
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
José Román Broullón
Email
joser.broullon.sspa@juntadeandalucia.es
Facility Name
Hospital General Universitario de Elche
City
Elche
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Elena Moreno
Email
elenamorenoperez@hotmail.com
Facility Name
Hospital Universitario de Getafe
City
Getafe
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sonia Diaz
Email
drasony@hotmail.com
Facility Name
Hospital Universitari Doctor Josep Trueta
City
Girona
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Maria Perez
Email
mperezdepuig@gmail.com
Facility Name
Hospital Sant Joan de Deu de Manresa
City
Manresa
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marina Alcoz
Email
marinalcoz@hotmail.com
Facility Name
Hospital Clínico Universitario Virgen de la Arrixaca
City
Murcia
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Maria Luisa Sanchez
Email
marisa00111@hotmail.com
Facility Name
Hospital Son Llàtzer
City
Palma De Mallorca
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Albert Tubau
Email
atubau68@icloud.com
Facility Name
Consorci Corporació Sanitària Parc Taulí de Sabadell
City
Sabadell
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Cristina Lesmes
Email
cristinalesmesheredia@gmail.com
Facility Name
Hospital Universitario Nuestra Señora de Candelaria
City
Santa Cruz De Tenerife
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Carolina Chulilla
Email
cchulilla@gmail.com
Facility Name
Hospital Universitario Virgen de Valme
City
Sevilla
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Carlota Borrero
Email
carlotaborrero@gmail.com
Facility Name
Hospital Universitari Joan XXIII
City
Tarragona
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lourdes Martin
Email
lourdesmartin3@hotmail.com
Facility Name
Hospital de Terrassa
City
Terrassa
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Esperanza Garcia
Email
egarciac@cst.cat
Facility Name
Hospital Universitari Mútua Terrassa
City
Terrassa
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Maria del Mar Pallarols
Email
mpallarols@mutuaterrassa.es
Facility Name
Hospital Universitario de Torrejon
City
Torrejón De Ardoz
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Irene Fernandez
Email
ibuhigas80@gmail.com
Facility Name
Hospital Clinico Universitario Lozano Blesa
City
Zaragoza
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Patricia Ibañez
Email
patribanez@hotmail.com

12. IPD Sharing Statement

Citations:
PubMed Identifier
36222789
Citation
Garcia-Manau P, Mendoza M, Bonacina E, Martin-Alonso R, Martin L, Palacios A, Sanchez ML, Lesmes C, Hurtado I, Perez E, Tubau A, Ibanez P, Alcoz M, Valino N, Moreno E, Borrero C, Garcia E, Lopez-Quesada E, Diaz S, Broullon JR, Teixidor M, Chulilla C, Gil MM, Lopez M, Candela-Hidalgo A, Salinas-Amoros A, Moreno A, Morra F, Vaquerizo O, Soriano B, Fabre M, Gomez-Valencia E, Cuina A, Alayon N, Sainz JA, Vives A, Esteve E, Ocana V, Lopez MA, Maroto A, Carreras E. The Fetal Growth Restriction at Term Managed by Angiogenic Factors Versus Feto-Maternal Doppler (GRAFD) Trial to Avoid Adverse Perinatal Outcomes: Protocol for a Multicenter, Open-Label, Randomized Controlled Trial. JMIR Res Protoc. 2022 Oct 11;11(10):e37452. doi: 10.2196/37452.
Results Reference
derived

Learn more about this trial

Management of Fetal Growth Restriction at Term: Angiogenic Factors Versus Feto-placental Doppler

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