Impact of Maternal Pomegranate Juice on Brain Injury in Infants With Intrauterine Growth Restriction (IUGR) (POM-1)
Primary Purpose
Intrauterine Growth Restriction
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Pomegranate Juice
Placebo
Sponsored by
About this trial
This is an interventional prevention trial for Intrauterine Growth Restriction focused on measuring Neuroprotection, Antioxidants, Neonatal brain injury, Pomegranate juice
Eligibility Criteria
Phase I:
Inclusion Criteria:
- Healthy expecting mothers two weeks from their expected due dates
- No evidence of IUGR
- No evidence of fetal problems
Phase II:
Inclusion Criteria:
- Expecting mother with a fetal diagnosis of intrauterine growth restriction (IUGR) defined by estimated fetal weight <10th percentile for gestational age
- 24 - 34 weeks gestation
Exclusion Criteria:
- Major congenital abnormalities
- Known fetal chromosomal disorder
- Maternal illicit drug use
- Maternal IV and Hepatitis C infection
- Premature rupture of membranes
Sites / Locations
- St Louis Children's Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Pomegranate juice
Placebo
Arm Description
This arm with receive 8oz of pomegranate juice per day.
This group will take 8oz of placebo juice that lacks pomegranate daily
Outcomes
Primary Outcome Measures
CNS injury at term by MR Imaging
Qualitative MRI injury- white matter injury (WMI) and gray matter injury (GMI)
Brain Metrics on MR imaging
Diffusion- apparent diffusion coefficient (ADC) and fractional anisotropy (FA)
Spectroscopy- lactate and NAA levels in the basal ganglia
Advanced MRI development indices - brain volumes, surface based morphology (SBM, folding indices)
Secondary Outcome Measures
Placental morphology: weight and size
Gestational age at delivery
Birth weight
Ellagic acid levels from cord blood
Dubowitz neurologic exam at term
Time to full oral feeds
ROP
NEC
Length of ventilatory support
Time to discharge
Placental micrography: number of villi, vasculature, collagen content
Placental immunohistochemistry: proliferation, apoptosis and differentiation
Placental: immunoassays: HSP90, lipid hydroperoxide, nitrotyrosine assay, paraoxonase 1 expression, superoxide dismutases
Placental RNA microarray
Umbilical cord gases
Pregnancy complications: preeclampsia
Neonatal wellbeing: APGAR scores, need for resuscitation
Full Information
NCT ID
NCT00788866
First Posted
November 10, 2008
Last Updated
October 16, 2014
Sponsor
Washington University School of Medicine
Collaborators
POM Wonderful LLC, University of California, Los Angeles
1. Study Identification
Unique Protocol Identification Number
NCT00788866
Brief Title
Impact of Maternal Pomegranate Juice on Brain Injury in Infants With Intrauterine Growth Restriction (IUGR)
Acronym
POM-1
Official Title
Impact of Maternal Pomegranate Juice on Brain Injury in Infants With Intrauterine Growth Restriction (IUGR)
Study Type
Interventional
2. Study Status
Record Verification Date
October 2014
Overall Recruitment Status
Completed
Study Start Date
December 2008 (undefined)
Primary Completion Date
October 2014 (Actual)
Study Completion Date
October 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Washington University School of Medicine
Collaborators
POM Wonderful LLC, University of California, Los Angeles
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Infants with intrauterine growth restriction are known to be at increased risk for long term neurodevelopmental delay into adulthood. The main mechanism for this is likely decreased blood flow to the brain secondary to altered placental blood flow. Antioxidants may serve to protect the developing brain from this process. Animal studies have shown that pomegranate juice protects the fetal brain from injury in a model of stroke. This clinical trial is intended to evaluate if giving mothers pomegranate juice during the last several weeks of pregnancy can help protect intrauterine growth restricted babies' brains.
Detailed Description
This study is divided into two separate phases.
Phase I evaluated if the antioxidants produced from pomegranate juice cross the placenta in normal healthy pregnancies. Twenty women were enrolled, 10 who will take 8 oz of pomegranate juice daily and then 10 others who will take 8 oz of placebo juice without pomegranate daily. Blood samples were first collected from the woman at the time enrollment and then from both the woman and the cord blood at the time of delivery. These blood samples were analyzed to measure the levels of antioxidant metabolites from the pomegranate juice. This phase was deigned to confirm placental transfer of antioxidant pomegranate metabolites. The results confirmed placenta transfer of pomegranate metabolites. Further, placental tissues from 12 patients (4 in the pomegranate group and 8 in the control group) were collected for analysis of oxidative stress. The preliminary in vivo results were extended to oxidative stress and cell death assays in vitro. Placental explants and cultured primary human trophoblasts were exposed to pomegranate juice or glucose (control) under defined oxygen tensions and chemical stimuli. We found decreased oxidative stress in term human placentas from women who labored after prenatal ingestion of pomegranate juice compared with apple juice as control. Moreover, pomegranate juice reduced in vitro oxidative stress, apoptosis, and global cell death in term villous explants and primary trophoblast cultures exposed to hypoxia, the hypoxia mimetic cobalt chloride, and the kinase inhibitor staurosporine. Punicalagin, but not ellagic acid, both prominent polyphenols in pomegranate juice, reduced oxidative stress and stimulus-induced apoptosis in cultured syncytiotrophoblasts.
Phase II focuses on pregnancies with intrauterine growth restriction. If they meet entry criteria, then woman will be enrolled and randomized into 1 of 2 groups.
Treatment group: Expecting mothers in this group will start a daily regimen of 8 oz glass of pomegranate juice. They will keep a daily diary documenting their compliance. They will continue this daily intake up until delivery of their infant.
Placebo group: These women will start a daily regimen of an 8 oz of pomegranate free juice placebo that matches taste, calories, and appearance to regular pomegranate juice but lacks polyphenols. They will also keep a diary of daily intake to help ensure compliance similar to the treatment group. They too will continue to take the placebos up until the time they deliver.
Both groups: All women will be followed up on a weekly basis to assess compliance. A detailed diet history will be collected from the women at the time of enrollment, midway through the 3rd trimester and at the time of delivery. Furthermore, all women will have a detailed social history collected at the time of enrollment. Upon delivery, cord blood will be collected and sent for ellagic acid, a polyphenic component. All placental material will be sent for formal pathological exam and analyzed for markers of placental injury.
If clinically stable, the infants will receive MRI evaluations to evaluate for possible brain injury.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Intrauterine Growth Restriction
Keywords
Neuroprotection, Antioxidants, Neonatal brain injury, Pomegranate juice
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
Care ProviderInvestigator
Allocation
Randomized
Enrollment
80 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Pomegranate juice
Arm Type
Experimental
Arm Description
This arm with receive 8oz of pomegranate juice per day.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
This group will take 8oz of placebo juice that lacks pomegranate daily
Intervention Type
Dietary Supplement
Intervention Name(s)
Pomegranate Juice
Intervention Description
8 oz of pomegranate juice daily vs placebo juice identical in all respects except pomegranate
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
Juice that matches the makeup of pomegranate in regards to sugar, vitamin C, etc. The only difference is that it lacks pomegranate juice.
Primary Outcome Measure Information:
Title
CNS injury at term by MR Imaging
Description
Qualitative MRI injury- white matter injury (WMI) and gray matter injury (GMI)
Brain Metrics on MR imaging
Diffusion- apparent diffusion coefficient (ADC) and fractional anisotropy (FA)
Spectroscopy- lactate and NAA levels in the basal ganglia
Advanced MRI development indices - brain volumes, surface based morphology (SBM, folding indices)
Time Frame
36 - 41 weeks (post delivery)
Secondary Outcome Measure Information:
Title
Placental morphology: weight and size
Time Frame
At birth
Title
Gestational age at delivery
Time Frame
At birth
Title
Birth weight
Time Frame
At birth
Title
Ellagic acid levels from cord blood
Time Frame
To discharge
Title
Dubowitz neurologic exam at term
Time Frame
To discharge
Title
Time to full oral feeds
Time Frame
To discharge
Title
ROP
Time Frame
To discharge
Title
NEC
Time Frame
To discharge
Title
Length of ventilatory support
Time Frame
To discharge
Title
Time to discharge
Time Frame
To discharge
Title
Placental micrography: number of villi, vasculature, collagen content
Time Frame
At birth
Title
Placental immunohistochemistry: proliferation, apoptosis and differentiation
Time Frame
At birth
Title
Placental: immunoassays: HSP90, lipid hydroperoxide, nitrotyrosine assay, paraoxonase 1 expression, superoxide dismutases
Time Frame
At birth
Title
Placental RNA microarray
Time Frame
At birth
Title
Umbilical cord gases
Time Frame
At birth
Title
Pregnancy complications: preeclampsia
Time Frame
At birth
Title
Neonatal wellbeing: APGAR scores, need for resuscitation
Time Frame
At birth
Other Pre-specified Outcome Measures:
Title
Maternal compliance
Description
Daily dietary report
Increase in polyphenol levels
Time Frame
To delivery
Title
Analysis both by 'intention to treat' and 'as treated'
Time Frame
To discharge
10. Eligibility
Sex
Female
Accepts Healthy Volunteers
No
Eligibility Criteria
Phase I:
Inclusion Criteria:
Healthy expecting mothers two weeks from their expected due dates
No evidence of IUGR
No evidence of fetal problems
Phase II:
Inclusion Criteria:
Expecting mother with a fetal diagnosis of intrauterine growth restriction (IUGR) defined by estimated fetal weight <10th percentile for gestational age
24 - 34 weeks gestation
Exclusion Criteria:
Major congenital abnormalities
Known fetal chromosomal disorder
Maternal illicit drug use
Maternal IV and Hepatitis C infection
Premature rupture of membranes
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael Nelson, MD, MPH
Organizational Affiliation
Washington University School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
St Louis Children's Hospital
City
St Louis
State/Province
Missouri
ZIP/Postal Code
63110
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
31433809
Citation
Matthews LG, Smyser CD, Cherkerzian S, Alexopoulos D, Kenley J, Tuuli MG, Nelson DM, Inder TE. Maternal pomegranate juice intake and brain structure and function in infants with intrauterine growth restriction: A randomized controlled pilot study. PLoS One. 2019 Aug 21;14(8):e0219596. doi: 10.1371/journal.pone.0219596. eCollection 2019.
Results Reference
derived
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Impact of Maternal Pomegranate Juice on Brain Injury in Infants With Intrauterine Growth Restriction (IUGR)
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