Cortisol Levels in Infants Born by C-section - Electric Unipolar Needle Versus Electric Bipolar Needle

Sponsor
Hadassah Medical Organization (Other)
Overall Status
Unknown status
CT.gov ID
NCT01100970
Collaborator
(none)
90
1
12
7.5

Study Details

Study Description

Brief Summary

The purpose of this study is to determine whether there is a difference between cortisol levels in fetal blood of babies who were born while using a unipolar needle opposite to using a bipolar needle, and compared to the control group (infants who were born in a vaginal birth).

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Today, on Caesarean section, there's a widely usage of electric unipolar needle for cutting tissue and / or bipolar needle to burn blood vessels. These Needles use an electric current flow for cutting the tissue. When using unipolar needle there's a transfer of the electric current through the mother's body and through the amniotic fluid , while when using bipolar needle the current goes back through the needle directly the generator so that the flow does not transfer to the amniotic fluid and fetus.

    Despite the growing usage of electric needles, there is no literature information about the extent of electrical current that is transferred to the fetus during cutting, hence, no information about stress level felt by the baby as a result of electrical current exposure.

    The purpose of this experiment is testing the possibility that there is a difference between cortisol levels in fetal blood of babies who were born while using a unipolar needle opposite to using a bipolar needle, and compared to the control group (infants who were born in a vaginal birth).

    Also, we want to check whether there is correlation between maternal cortisol levels and newborn cortisol levels (whether motherly cortisol levels affects newborn cortisol levels).

    To assess cortisol at birth, blood will be taken from the umbilical vein following clamping of the cord after birth. Saliva-based cortisol will be collected from mothers.

    Other measures which will be taken are: week of birth, newborns weight, Apgar score 5 minutes after birth, mother's age and the indication for cesarean section.

    Then we will compare the two experimental groups, as well as compare the two groups, to the control group, and see whether there is a statistically significant difference between the groups.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    90 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Cortisol Levels in Infants Born by C-section - A Comparison of Using an Electric Unipolar Needle and Electric Bipolar Needle
    Study Start Date :
    May 1, 2010
    Anticipated Primary Completion Date :
    May 1, 2011
    Anticipated Study Completion Date :
    May 1, 2011

    Arms and Interventions

    Arm Intervention/Treatment
    Unipolar electric needle

    Bipolar electric needle

    Control

    Infants who were born in a vaginal birth

    Outcome Measures

    Primary Outcome Measures

      Eligibility Criteria

      Criteria

      Ages Eligible for Study:
      20 Years to 45 Years
      Sexes Eligible for Study:
      Female
      Accepts Healthy Volunteers:
      Yes
      Inclusion Criteria:
      1. Healthy women, without significant background and/or chronic diseases.

      2. Women who did not experienced illnesses that may pass to the fetus during pregnancy, or any other medical complication related to pregnancy.

      3. All indications for C-section are medical indications.

      4. Male newborn, week 37-42 of pregnant.

      5. Without any evidence of stress event suffered by the mother or fetus during pregnancy or at birth.

      Exclusion Criteria:
      1. Women over 45 years of age, or under the age of 20.

      2. Women with significant background and/or chronic diseases.

      3. Women who experienced medical complications during pregnancy.

      4. C-section indication are urgent due to mother/fetus distress.

      5. Female newborn, or a male newborn who wasn't born during week37-42 of pregnancy.

      6. Evidence of a stress event suffered by the mother and/or fetus during pregnancy or at birth.

      Contacts and Locations

      Locations

      Site City State Country Postal Code
      1 Hadassah Medical Organization Jerusalem Israel 91120

      Sponsors and Collaborators

      • Hadassah Medical Organization

      Investigators

      • Principal Investigator: David Mankuta, MD, Hadassah University Medical Organization

      Study Documents (Full-Text)

      None provided.

      More Information

      Publications

      Responsible Party:
      , ,
      ClinicalTrials.gov Identifier:
      NCT01100970
      Other Study ID Numbers:
      • 0008-10HMO-CTIL
      First Posted:
      Apr 9, 2010
      Last Update Posted:
      Feb 1, 2011
      Last Verified:
      Feb 1, 2010

      Study Results

      No Results Posted as of Feb 1, 2011