NCT00425867

Brief Summary

The present study will be undertaken to establish whether genetic variations of PAR1 could be involved in the occurrence of any of the "placental syndromes" of preterm delivery, preeclampsia, and/or small for gestational age babies and recurrent pregnancy loss.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Mar 2007

Shorter than P25 for all trials

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 22, 2007

Completed
1 day until next milestone

First Posted

Study publicly available on registry

January 23, 2007

Completed
1 month until next milestone

Study Start

First participant enrolled

March 1, 2007

Completed
8 months until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2007

Completed
Last Updated

January 26, 2007

Status Verified

January 1, 2007

First QC Date

January 22, 2007

Last Update Submit

January 25, 2007

Conditions

Miscarriage, RecurrentPremature Labor

Keywords

PAR1 genepolymorphismsabortionsreccurent abortionspremature delivery

Interventions

PAR1 polymoprhisms and placental invasionBEHAVIORAL

Eligibility Criteria

Age20 Years - 40 Years
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Women with reccurent abortions unexplained
  • Premature delicery

You may not qualify if:

  • Term pregnancies
  • Abortion that the cause is known

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Links

MeSH Terms

Conditions

Abortion, HabitualObstetric Labor, PrematurePremature Birth

Condition Hierarchy (Ancestors)

Abortion, SpontaneousPregnancy ComplicationsFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesObstetric Labor Complications

Study Officials

  • Sorina Grisaru, MD

    Shaare Zedek Medical Center

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Sorina Grisaru, MD

CONTACT

97226555111granovsky@netvision.net.il

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
OTHER
Sponsor Type
OTHER

Study Record Dates

First Submitted

January 22, 2007

First Posted

January 23, 2007

Study Start

March 1, 2007

Study Completion

November 1, 2007

Last Updated

January 26, 2007

Record last verified: 2007-01