Autopsy report · NCT02212210

Maternal Epidural Steroids and Hyperthemia

“PI permanently closed accrual for the study based on FDA warning issued in April 2014. Study is closed”

The sponsor’s own words in the registry.

Life of this trial

• Registered 2 years 6 months after it had already started.
• Ran for about 3 years 8 months before it stopped.
• 135 participants enrolled.
• No results are posted on the registry.

Vital statistics

Status

Terminated

Phase

Early Phase 1

Sponsor

Medical University of South Carolina

Sponsor type

University, hospital or other

Conditions

Fever; Labor Pain; Complication of Anesthesia During Pregnancy, Unspecified

Interventions

Methylprednisolone; Normal saline

Participants

135

Sites

1

Countries

United States

Trials that died the same way

• Superficial Cervical Plexus Block for Improved Outcomes in Pediatric Otolaryngologic Surgery
  “The current PI is leaving the study. Study team is awaiting FDA PI change approval.” (74% match in meaning)
• Subcutaneous Recombinant Human Hyaluronidase: Workflow Analysis and Emergency Department Design
  “This study was closed before accrual due to FDA recall of Medication” (71% match in meaning)
• Endocrine Therapy + OSI-906 With or Without Erlotinib for Hormone-Sensitive Metastatic Breast Cancer
  “PI closed study early, all patients experienced severe toxicities and progressed” (70% match in meaning)
• A Safety and Effectiveness Study of Immediate Release Tapentadol Hydrochloride Among Filipino Patients With Moderate to Severe Acute Non-Cancer Pain
  “The company decided to cancel this study in conformity with PH FDA Circular 2013-004” (68% match in meaning)
• Dual Antiplatelet Therapy Adherence With Reminder App Usage
  “The PI is discontinuing the study since the platform/Application is no longer available for use. Study terminated effective 7/29/2024.” (68% match in meaning)

Look deeper

• The official registry record (the source of truth)
• Record history: every change the sponsor made
• Open it in the database

Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.