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A Prospective, Noninterventional Follow-Up Study of Children Aged 23 to 25 Months, Born to Mothers Who Received Hydroxyprogesterone Caproate Injection, 250 mg/mL, or Vehicle for Prevention of Preterm Birth

This study is currently recruiting participants.
Verified December 2015 by Lumara Health, Inc.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01146990
First Posted: June 22, 2010
Last Update Posted: December 11, 2015
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. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
Collaborator:
Registrat-Mapi
Information provided by (Responsible Party):
Lumara Health, Inc.
No Study Results Posted on ClinicalTrials.gov for this Study
  Study Status: This study is currently recruiting participants.
  Estimated Study Completion Date: October 2020
  Estimated Primary Completion Date: August 2020 (Final data collection date for primary outcome measure)