TEMPURA: Thromboelastometry Prediction Utility for Risk of Abortion

Sponsor
Icahn School of Medicine at Mount Sinai (Other)
Overall Status
Completed
CT.gov ID
NCT03548701
Collaborator
(none)
98
1
11.3
8.6

Study Details

Study Description

Brief Summary

This study will use thromboelastometry in ED patients with vaginal bleeding, as well as healthy pregnant controls, to determine if abnormal results are associated with the presence of vaginal bleeding as well as later complications during pregnancy.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Thromboelastometry testing

Detailed Description

First, a case control study with samples collected from patients in the ED and OB clinic at Mount Sinai Hospital will be performed. Blood samples are being collected at time of study entry. Patient health history will be collected and blood samples will be tested using thromboelastometry in prospective fashion. Samples will be compared between groups.

A prospective cohort will then be established using the subjects from the case control study. The purpose of this prospective cohort will be to collect outcomes of pregnancies to determine association with the initial thromboelastometry results.

Study Design

Study Type:
Observational
Actual Enrollment :
98 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
Thromboelastometry Prediction Utility for Risk of Abortion
Actual Study Start Date :
Jun 4, 2018
Actual Primary Completion Date :
May 15, 2019
Actual Study Completion Date :
May 15, 2019

Arms and Interventions

Arm Intervention/Treatment
Emergency Department

Patients enrolled in the Emergency Department undergoing evaluation for threatened abortion abnormalities.

Diagnostic Test: Thromboelastometry testing
Thromboelastometry testing - a form of testing in whole blood for coagulation abnormalities

Obstetric Clinic

Patients with normal pregnancies being treated at first obstetric visit in clinic.

Diagnostic Test: Thromboelastometry testing
Thromboelastometry testing - a form of testing in whole blood for coagulation abnormalities

Outcome Measures

Primary Outcome Measures

  1. Maximum Clotting Firmness (MCF) [Day 1]

    Thromboelastometry measurement of the Maximum Clot Firmness over the duration of the test. Performed as part of InTEM (response to ellagic acid) and ExTEM (response to tissue factor) measures.

Secondary Outcome Measures

  1. Clot formation time (CFT) [Day 1]

    Time to thromboelastometry measurement of the angle between formation of clot at 0mm and 20mm of strength. Performed as part of InTEM (response to ellagic acid) and ExTEM (response to tissue factor) measures.

  2. Clotting Time (CT) [Day 1]

    Thromboelastometry measurement of the time to first clot formation. Performed as part of InTEM (response to ellagic acid) and ExTEM (response to tissue factor) measures.

  3. Pregnancy Outcome [Within 40 weeks of enrollment at completion of pregnancy]

    Assessment of pregnancy outcome. Variable is treated as categorical and coded as spontaneous abortion, preterm labor, or term labor.

  4. Number of Pregnancy Complications [Within 40 weeks of enrollment at completion of pregnancy]

    Number of Pregnancy complications as a composite including pre-eclampsia, postpartum hemorrhage, or other clotting or bleeding dysfunction such as pulmonary embolus or preterm bleeding episodes.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Subjects will include pregnant women seen in the ED and OB clinic.

The ED patients will include those seen for vaginal bleeding during pregnancy at less than 20 weeks gestation.

OB Clinic patients will include those seen for first prenatal visit at which blood draw is performed, as long as this is also within 20 weeks estimated gestational age.

Exclusion Criteria:
  • Patients with known histories of recurrent miscarriage, previously diagnosed thrombophilia, or other coagulopathy will be excluded.

  • Patients with ectopic pregnancies will also be excluded.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Mount Sinai Hospital New York New York United States 10029

Sponsors and Collaborators

  • Icahn School of Medicine at Mount Sinai

Investigators

  • Principal Investigator: Patrick J Maher, MD, Icahn School of Medicine at Mount Sinai

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Patrick Maher, Assistant Professor, Icahn School of Medicine at Mount Sinai
ClinicalTrials.gov Identifier:
NCT03548701
Other Study ID Numbers:
  • GCO 18-0104
First Posted:
Jun 7, 2018
Last Update Posted:
Jun 1, 2020
Last Verified:
May 1, 2020
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Patrick Maher, Assistant Professor, Icahn School of Medicine at Mount Sinai
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 1, 2020