Sonographic Prediction of Preterm Delivery Between 24-34 Weeks of Gestation

The recruitment status of this study is unknown because the information has not been verified recently.
Verified January 2008 by Soroka University Medical Center.
Recruitment status was  Active, not recruiting
Sponsor:
Information provided by:
Soroka University Medical Center
ClinicalTrials.gov Identifier:
NCT00613210
First received: January 22, 2008
Last updated: February 11, 2008
Last verified: January 2008
  Purpose

to evaluate if sonographic measure of short uterin cervix, sludge in amniotic fluid and abnormal doppler of the uterin artery can predict preterm labor


Condition
Healthy

Study Type: Observational
Study Design: Observational Model: Case Control
Time Perspective: Prospective
Official Title: Sonographic Prediction of Preterm Delivery Between 24-34 Weeks of Gestation

Further study details as provided by Soroka University Medical Center:

Biospecimen Retention:   None Retained

sonographic measurments


Estimated Enrollment: 150
Study Start Date: January 2008
Estimated Primary Completion Date: June 2008 (Final data collection date for primary outcome measure)
Groups/Cohorts
1
women without contraction at 24-34 weeks of gestation
2
women without contractions between 24-34 weeks of gestation with a history of preterm labor
3
women with preterm contractions 24-34 weeks of gestation

  Eligibility

Ages Eligible for Study:   18 Years to 40 Years
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population

women that visit a tetriary hospital for follow up

Criteria

Inclusion Criteria:

  • pregnancy between 24-34 wees of gestation

Exclusion Criteria:

  • lack prenatal care
  • fetal malformations stractural or genetical
  • plcenta previa
  • cerclage
  • women who underwent conization of cervix
  • polyhydramnious
  • premature rupture of membranes
  • induction of labor d/t medical condition preterm
  • women with hypertension, diabetis or preeclampsia
  • susp IUGR
  • women with a chronic illness that may interupt pregnancy
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00613210

Sponsors and Collaborators
Soroka University Medical Center
Investigators
Principal Investigator: Limor Man soroka medical center sonar unit of obstetrics and gynecology department
Principal Investigator: limor man, MD Soroka Medical Center
  More Information

No publications provided

Responsible Party: Limor Man, soroka medical center
ClinicalTrials.gov Identifier: NCT00613210     History of Changes
Other Study ID Numbers: SOR463907CTIL, 4639
Study First Received: January 22, 2008
Last Updated: February 11, 2008
Health Authority: Israel: minestry of health

Keywords provided by Soroka University Medical Center:
preterm delivery
shory cervix
amniotic fluid sludge
uterine artery doppler
singeltone
normal amniotic fluid index
without rupter of membranes
24-34 weeks of gestation

Additional relevant MeSH terms:
Premature Birth
Obstetric Labor Complications
Obstetric Labor, Premature
Pregnancy Complications

ClinicalTrials.gov processed this record on October 22, 2014