Comprehensive Pain Management Center
One Hospital Dr
Columbia, 65212-0001
United States
Neonatology (Newborn Intensive Care)
Neonatology (Newborn Intensive Care)
Medicine - Psychiatry (Mental Wellness)
Neonatology (Newborn Intensive Care)
Neonatology (Newborn Intensive Care)
Neonatology (Newborn Intensive Care)
Neonatology (Newborn Intensive Care)
One Hospital Dr
Columbia, 65212-0001
United States
Neonatology (Newborn Intensive Care)
The purpose of the study is to test the use of a drug called bromocriptine for women who have a condition called Peripartum cardiomyopathy; or PPCM. PPCM means you have a weak heart after giving birth. The study will look at how the heart muscle improves in women taking bromocriptine compared to a group of women given a placebo or inactive pill. Bromocriptine is approved by the United States Food and Drug Administration (FDA) to treat irregular periods and other symptoms that result from having high blood levels of a substance called prolactin. It is not approved for use in usual care to treat PPCM.
Study ID: 3330
NCT Number: NCT05180773
Principal Investigator:
Karen Florio, DO
Department: Ob, Gyn & Women's Health
Eligibility: Women 18 years old to 100 years old. Does not accept healthy volunteers.
For questions about this study, please contact:
ClinicalTrialsInterest@health.missouri.eduNeonatology (Newborn Intensive Care)
Neonatology (Newborn Intensive Care)
The U.S. Food and Drug Administration (FDA) has approved the steroid dexamethasone for both oral consumption, and injections through the following routes: intravenous, intramuscular, intraarticular, soft tissue, and intralesional. Dexamethasone is commonly used in surgery, but its use is generally up to the discretion of the treating physician whether it is used in lumbar disc herniation surgeries or not as this is an off-label use of dexamethasone not currently approved by IRB Approval Date: Sep 04, 2024; Written Consent with HIPAA Authorization ID #737119; Amendment ID #430440 VERSION 16, 8/29/2024 3 of 13 the FDA. In this study we would like to learn more about which patient population benefits the most from utilization of this drug intra-operatively after lumbar disc herniation.
Study ID: 1866
NCT Number: NCT04182997
Principal Investigator:
Don Moore, MD
Department: Orthopaedic Surgery
Eligibility: Both men and women 18 years old to 100 years old. Does not accept healthy volunteers.
For questions about this study, please contact:
ClinicalTrialsInterest@health.missouri.eduNeonatology (Newborn Intensive Care)
Neonatology (Newborn Intensive Care)
Neonatology (Newborn Intensive Care)
Neonatology (Newborn Intensive Care)
General Pediatrics
Neonatology (Newborn Intensive Care)
Neonatology (Newborn Intensive Care)
Neonatology (Newborn Intensive Care)
Neonatology (Newborn Intensive Care)
Neonatology (Newborn Intensive Care)
Nurse Manager, Neonatal Intensive Care Unit
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