Autopsy report · NCT05289466

Oncoplastic Partial Mastectomy With Intraoperative Radiation Therapy (IORT) in Early Stage Breast Cancer Patients With Prior History of Chest Wall Radiation.

“Internal research admin issue required this study to be closed, will re-open an amended protocol.”

The sponsor’s own words in the registry.

Life of this trial

• Registered 3 months after it had already started.
• Ran for about 2 years 10 months before it stopped.
• 5 participants enrolled.
• No results are posted on the registry.

Vital statistics

Status

Terminated

Phase

Na

Sponsor

Saint John's Cancer Institute

Sponsor type

University, hospital or other

Conditions

IORT-Intra-Operative Radiation Therapy

Interventions

Intraoperative Radiotherapy; Oncoplastic partial mastectomy

Participants

5

Sites

1

Countries

United States

Trials that died the same way

• Inhaled Sodium Nitrite as an Antimicrobial for Cystic Fibrosis
  “Protocol closed due to difficulty recruiting subjects and then expiration of investigational product and lack of a manufacturer.” (63% match in meaning)
• Safety and Effectiveness Study of RF Ablation of Uterine Fibroids to Reduce Menstrual Bleeding: the Fibroid Ablation Study
  “study revised and reinitiated under another protocol” (61% match in meaning)
• Effect of HAART Vs. Statin Treatment on Endothelial Function and Inflammation/Coagulation
  “On 05/08/12, team working on revising protocol and re-open study under version 2.0” (60% match in meaning)
• Effects of Whole Food, Plant-Based Nutrition on Chronic Kidney Disease With Proteinuria
  “Substantially redesigning study protocol and opening a new study in the future.” (60% match in meaning)
• Estimate Serum Oxytocin PD Range in the Periphery
  “Study will be replaced by a revised study protocol” (60% 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.