Autopsy report · NCT02441439

To Compare the Efficacy of I.V 200 mg Iron Sucrose and 500 mg Iron Sucrose to Treat Anemia in Pregnancy

“The investigators decided not to proceed with this study”

The sponsor’s own words in the registry.

Life of this trial

• Withdrawn before it enrolled anyone. Its dates are the sponsor's plans, not events that happened.

Vital statistics

Status

Withdrawn

Phase

Na

Sponsor

HaEmek Medical Center, Israel

Sponsor type

University, hospital or other

Conditions

Pregnancy

Interventions

Iron sucrose 200 mg; Iron sucrose 500 mg

Participants

0

Trials that died the same way

• Activity of Pre-Osteoclasts and Osteoclasts Over Time in Postmenopausal Women Treated With Denosumab or Zoledronic Acid
  “The Investigator decided not to pursue this study.” (90% match in meaning)
• Effect of an Intervention Based on Back School in an Aquatic Environment on Non-specific Low Back Pain
  “The study was not initiated following an investigator decision not to proceed; no participants were enrolled.” (82% match in meaning)
• The Effects of Active VItamin D on Left Atrial Volume Index
  “Investigator decided not to pursue.” (79% match in meaning)
• Magnetic Resonance-guided High-Intensity Focused Ultrasound (MR-HIFU) Used for Mild Hyperthermia
  “Decision was made to not go forward with the study” (78% match in meaning)
• Effect of Longer-term Adrenal Suppression Using Low Dose Hydrocortisone on Androgen Overproduction
  “The study team decided not to pursue this study.” (77% 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.