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Status unknownNCT02901340Updated Sep 15, 2016

Fetal Renal Artery Doppler Indices in Borderline Isolated Oligohydramnios

An observational study in Oligohydramnios, sponsored by Kayseri Education and Research Hospital. Status unknown at 1 site in Turkey. Open to female participants aged 18 Years to 35 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2016-09-15.

Sponsored by Kayseri Education and Research Hospital · Observational

The sponsor has not verified this record recently (last verified Sep 2016), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
140
Ages
18 Years to 35 Years
Sex
Female
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Study summary

The purpose of the study is to investigate third trimester fetal renal artery doppler indices in borderline idiopathic isolated oligohydramnios and relationship between neonatal outcomes.

Read the detailed description

During a routine pregnancy examination at 34-37 weeks gestation, the fetus was evaluated using ultrasound with the Toshiba Xario 200 3.5-megahertz probe. Fetal biometric measurements were obtained and placental structure and the amniotic fluid amount were evaluated in four quadrants. After detailed ultrasonography of the fetus, eligible pregnant women were included in the study.

Borderline idiopathic isolated oligohydramnios was defined according to the four quadrants technical with ultrasound examination and diagnosed with amniotic fluid index >5.0 and ≤8.0cm. After first ultrasound examination all patients in borderline isolated oligohydramnios group were hydrated with one to two liters of water daily. All patients monitored with non stress test and amniotic fluid index twice weekly until delivery after treatment with hydration.

For evaluating renal artery blood flow, an axial image of the fetal abdomen was obtained at the level of the fetal kidneys. Using color flow Doppler, the renal arteries were evaluated at the level of their origin from the abdominal aorta. The Doppler gate was placed within the lumen in a straight segment of the vessel. A minimum of three consecutive waveforms was used to calculate the PI. The umbilical artery Doppler measurements were studied in a free loop of cord, far from the fetus and placenta. pulsatile index and resistance index values were recorded.

The study consisted of two groups. The first group was formed of the patients who had normal amniotic volume and meets the inclusion criteria. In second group the investigators included patients who diagnosed borderline idiopathic isolated oligohydramnios. After delivery the investigators compared fetal renal artery doppler indices and neonatal outcomes between groups.

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Conditions studied

  • Oligohydramnios

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Keywords

  • Borderline idiopathic isolated oligohydramnios
  • Fetal renal artery doppler indices
  • neonatal outcomes
  • Maternal hydration
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In context

Oligohydramnios

25 studies on the registry are indexed under Oligohydramnios; 5 are open to participants now.

Browse Oligohydramnios studies →

Lead sponsor

Kayseri Education and Research Hospital is the lead sponsor of 27 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 35 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

The study population was consisted of 2 groups and included pregnant women in between 34 and 37. weeks of gestation for both groups. The normal pregnancy group was consisted of 100 healthy pregnant women whom excluded borderline idiopathic isolated oligohydramniosis , the main group was consisted of 40 pregnant women with diagnosed borderline idiopathic isolated oligohydramniosis.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • singleton pregnancies
  • between 34-37 gestational weeks
  • the age of them ranged from 18 to 35 years

Exclusion criteria

Exclusion Criteria:

  • uteroplacental insufficiency
  • preeclampsia
  • chronic hypertension
  • collagen vascular disease
  • nephropathy
  • chromosomal abnormalities
  • congenital abnormalities, especially those associated with impaired urine production
  • growth restriction
  • ruptured fetal membranes
  • twin pregnancies
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Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
140 participants (estimated)
Patient registry
No

Groups and cohorts

  • Borderline isolated oligohydramnios

    Borderline idiopathic isolated oligohydramnios was defined according to the four quadrants technical with ultrasound examination and diagnosed with amniotic fluid index\>5.0 and ≤8.0cm. The borderline idiopathic isolated oligohydramnios group was formed of the patients who meets the inclusion criteria and between 34-37 weeks gestation (n:40)

    Dietary Supplement: one to two liters of water daily

  • Control group

    The control group was formed of the patients who had normal amniotic volume and 34-37 weeks gestation who meets the inclusion criteria (n:100)

Interventions

  • Dietary supplementone to two liters of water daily
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What researchers measure

Primary outcomes

  1. Fetal renal artery pulsatile index in borderline idiopathic isolated oligohydramnios

    Time frame: 4 months

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Study locations

1 of 1 sites recruiting
  • Kayseri Training and Research Hospital
    Kayseri, 38000, Turkey
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 15, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02901340
Lead sponsor
Kayseri Education and Research Hospital
Responsible party
Erdem Sahin (Principal Investigator, Kayseri Education and Research Hospital) — Principal investigator
First posted
Sep 15, 2016
Start date
Aug 2016
Primary completion
Dec 2016 (estimated)
Completion
Dec 2016 (estimated)
Last update
Sep 15, 2016

Study contacts

Erdem SAHİN, Study Principal İnvestigator
Contact
erdemsahin07@hotmail.com
+095321688683
View the source record on ClinicalTrials.gov ↗

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This study is status unknown, as verified in Sep 2016. You cannot join it, but the record below documents what was studied.

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