We updated the design of this site on September 25th. Learn more.
Show more
ClinicalTrials.gov
ClinicalTrials.gov Menu

Intrapartum Fever and Histopathological Placental Findings

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified August 2010 by Wolfson Medical Center.
Recruitment status was:  Enrolling by invitation
Sponsor:
ClinicalTrials.gov Identifier:
NCT01175187
First Posted: August 4, 2010
Last Update Posted: August 10, 2010
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Wolfson Medical Center
  Purpose
Intrapartum fever associated with epidural anesthesia is caused by non infectious causes therefore without histological findings

Condition Phase
Histological Placental Inflamation With or Without Fever Phase 4

Study Type: Observational
Study Design: Observational Model: Case Control
Time Perspective: Retrospective
Official Title: Intrapartum Fever and Histopathological Placental Findings

Resource links provided by NLM:


Further study details as provided by Wolfson Medical Center:

Biospecimen Description:
degree and location of inflamation

Enrollment: 200
Study Start Date: April 2009
Estimated Study Completion Date: October 2010
Estimated Primary Completion Date: March 2010 (Final data collection date for primary outcome measure)
Groups/Cohorts
EPIDURAL FEVER
EPIDURAL WITHOUT FEVER
GROUP 1: EPIDURAL FEVER . GROUP 2 EPIDURAL WITHOUT FEVER

  Eligibility

Information from the National Library of Medicine

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, Learn About Clinical Studies.


Ages Eligible for Study:   18 Years to 40 Years   (Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Sampling Method:   Probability Sample
Study Population
200 normal deliveries
Criteria

Inclusion Criteria:epidural with and without fever

Exclusion Criteria:

  • Patients with infectious backgroud or prilinged PROM
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01175187


Sponsors and Collaborators
Wolfson Medical Center
Investigators
Principal Investigator: shmuel evron, md Tel Aviv University
  More Information

Responsible Party: ob&anesth Unit, wolfson medical center
ClinicalTrials.gov Identifier: NCT01175187     History of Changes
Other Study ID Numbers: 1077
First Submitted: August 2, 2010
First Posted: August 4, 2010
Last Update Posted: August 10, 2010
Last Verified: August 2010

Keywords provided by Wolfson Medical Center:
evron

Additional relevant MeSH terms:
Fever
Body Temperature Changes
Signs and Symptoms