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Clinical Trials/NCT04523233
NCT04523233
Unknown
Not Applicable

Maternal Plasma/Urine/Hair/Amniotic Fluid Levels of Selected Trace Elements and Heavy Metals in Pregnancies Complicated With Neural Tube Defects

Cengiz Gokcek Women's and Children's Hospital1 site in 1 country140 target enrollmentAugust 25, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Neural Tube Defects
Sponsor
Cengiz Gokcek Women's and Children's Hospital
Enrollment
140
Locations
1
Primary Endpoint
elements/vitamins concentrations in both group
Last Updated
4 years ago

Overview

Brief Summary

Introduction: Heavy metals important pollutants produced from anthropogenic activities, has been suggested to be embryotoxic and fetotoxic in a lot of studies. The aims of this study were to determine the levels of trace elements and heavy metals, namely folic acid, zinc (Zn), molybdenum (Mo), vanadium (V), strontium (Sr), aluminium (Al), tin (Sn), antimony (Sb), mercury (Hg), calcium (Ca), iron ( Fe), magnesium (Mg), phosphorus (P), barium (B) and selenium (Se), in the amniotic fluid of pregnant women, and to investigate their relationship with neural tube defects (NTDs).

Methods: The study will be included 70 pregnant women whose fetuses were complicated with NTDs (study group) and 70 pregnant women with unaffected healthy fetuses (control group). The samples levels of elements and vitamins will be measured using inductively coupled plasma-mass spectrometry and will be compared between the two groups.

Detailed Description

Detailed Description: This observational case-control study will be conducted at the Department of Obstetrics and Gynecology, Cengiz Gokcek Public Hospital, Gaziantep, Turkey, between August 2020 and March 2021. The protocol was approved by the Ethics Committee for Clinical Research of Gaziantep University (reference no: 2020/167). The study strictly will be adhered to the principles of the Declaration of Helsinki. All women will be provided written informed consent before the acquisition of all samples. The study will be included 140 pregnant women who underwent amniocentesis at the investigator's perinatology department. The study group will be included 70 pregnant women whose fetuses were found to have congenital NTDs (eg, anencephaly, spina bifida, acrania, and encephalocele) on detailed ultrasonographic examinations between 16 and 37 weeks of pregnancy. The control group included pregnant women with healthy fetuses (n = 70), who were matched for gestational weeks and maternal age and underwent amniocentesis because of age-related risk or increased risk in the triple test. Then, this study will be determined maternal plasma/urine/hair, and amniotic fluid folic acid, zinc (Zn), molybdenum (Mo), vanadium (V), strontium (Sr), aluminium (Al), tin (Sn), antimony (Sb), mercury (Hg), calcium (Ca), iron ( Fe), magnesium (Mg), phosphorus (P), barium (B) and selenium (Se) concentrations in women with NTD compared to those of volunteer healthy pregnant women.

Registry
clinicaltrials.gov
Start Date
August 25, 2020
End Date
February 28, 2022
Last Updated
4 years ago
Study Type
Observational
Sex
Female

Investigators

Sponsor
Cengiz Gokcek Women's and Children's Hospital
Responsible Party
Principal Investigator
Principal Investigator

Ali Ovayolu

Principal Investigator

Cengiz Gokcek Women's and Children's Hospital

Eligibility Criteria

Inclusion Criteria

  • Pregnant women complicated with Neural tube defects
  • Healthy pregnancy
  • Singleton pregnancy

Exclusion Criteria

  • pregnant women with any systemic condition (such as chronic hypertension, renal disease and )
  • women who have dyed their hair in the last 5 months
  • history of using any medication
  • presence of gestational hypertension or gestational diabetes
  • patients who had other fetal congenital abnormalities or genetic syndromes
  • multiple-gestation pregnancies
  • intrauterine fetal death
  • oligohydramnios

Outcomes

Primary Outcomes

elements/vitamins concentrations in both group

Time Frame: 1 week

The primary outcome in these analyses will compare folic acid, zinc (Zn), molybdenum (Mo), vanadium (V), strontium (Sr), aluminum (Al), tin (Sn), antimony (Sb), mercury (Hg), calcium (Ca), iron ( Fe), magnesium (Mg), phosphorus (P), barium (B) and selenium (Se) concentrations in NTD group and control group.

Secondary Outcomes

  • compore in NTDs group(1 week)

Study Sites (1)

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