Autopsy report · NCT05440084

Impact of CTO PCI (Chronic Total Occlusion Percutaneous Intervention) on Regular Physical Activity

“Recruitment not possible in study location given study population.”

The sponsor’s own words in the registry.

Life of this trial

• Registered 2 months before it started.
• Ran for about 2 years before it stopped.
• 1 participant enrolled.
• No results are posted on the registry.

Vital statistics

Status

Terminated

Sponsor

Minneapolis Heart Institute Foundation

Sponsor type

University, hospital or other

Conditions

Chronic Total Occlusion; Occlusion

Interventions

Chronic total occlusion percutaneous coronary intervention

Participants

1

Sites

1

Countries

United States

Trials that died the same way

• Combined CT Colonography and PET Imaging in Mantle Cell Lymphoma
  “No study recruitment due to time constraints and lack of support.” (78% match in meaning)
• The Role of Ursodeoxycholic Acid in Treatment of Gallstones in Hemolytic Disorders
  “Study not feasible - very low recruitment rate” (75% match in meaning)
• Hypoxia and Heart Rate Variability
  “Study stopped due to no recruitment activities” (74% match in meaning)
• Biliary Interventions in Critically Ill Patients With Secondary Sclerosing Cholangitis (BISCIT)
  “Study was stopped due to insufficient recruitment.” (74% match in meaning)
• Randomized, Blinded, Sham-controlled Trial of Acupuncture for the Management of Joint Pain in Patients With Psoriasis
  “Not enough study participants, difficulties in recruitment” (73% 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.