Autopsy report · NCT00382863

Prospective Evaluation of Elastic Restraint to LESSen the Effects of Heart Failure (PEERLESS-HF) Trial

“Resources unavailable to continue study follow-up.”

The sponsor’s own words in the registry.

Life of this trial

• Ran for about 5 years 7 months before it stopped.
• 220 participants enrolled.
• Results were posted on the registry 2 months after it ended.

Vital statistics

Status

Terminated

Phase

Phase 2, Phase 3

Sponsor

Paracor Medical, Inc

Sponsor type

Industry

Conditions

Heart Failure

Interventions

HeartNet Ventricular Support System; Optimal Medical/Device Therapy

Participants

220

Sites

35

Countries

Canada, United States

Trials that died the same way

• Remote Monitoring of Respiratory Health
  “Resources not available to continue study” (85% match in meaning)
• Home-based SSP on Individuals With PWS
  “Insufficient resources to complete study as planned” (72% match in meaning)
• Noninvasive NAVA Versus NIPPV in Low Birthweight Premature Infants
  “Insufficient resources available to complete the study” (68% match in meaning)
• Prospective Comparison of Revolve™ and AuraGen 123 With AuraClens™ in Autologous Fat Grafting to the Breast
  “Study discontinued due to lack of subject follow-up.” (67% match in meaning)
• HBOT Late Radiation Tissue Injury
  “Lack of resources to complete the study” (67% 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.