Autopsy report · NCT04855227

A Prospective Evaluation of Pain After Non-complex Ventral Hernia Repair

“Slow rate of enrollment . Additionally it was observed during the course of the trial that changes to the standard of care pain management protocols at some of the institutions, which are not aligned with the study protocol requirements”

The sponsor’s own words in the registry.

Life of this trial

• Registered 5 months before it started.
• Ran for about 3 years 3 months before it stopped.
• 69 participants enrolled.
• No results are posted on the registry.

Vital statistics

Status

Terminated

Sponsor

Intuitive Surgical

Sponsor type

Industry

Conditions

Ventral Hernia

Interventions

robotic-assisted ventral hernia repair

Participants

69

Sites

1

Countries

United States

Trials that died the same way

• Intranasal Fentanyl Versus Oral Morphine Sulfate in the Treatment of Pain in Pediatric Trauma
  “The new pain protocols imposed by the HAS make it difficult to include new patients in the study” (72% match in meaning)
• Study Testing Radium-223 Dichloride in Relapsed Multiple Myeloma
  “Due to the changes of standard of care and the slow recruitment of participants.” (64% match in meaning)
• Use of 3M Cavilon Advanced Skin Protectant in the Management of Damaged Skin Around an Ostomy, Drain or Fistula
  “Slow enrollment of patients” (62% match in meaning)
• Allogeneic Donor Lymphocyte Infusions Combined With Blinatumomab
  “Lack of potential study subjects due to a change of standard of care treatment outside of clinical trials.” (62% match in meaning)
• Study of Sotatercept for the Treatment of Chemotherapy Induced Anemia in Patients With Metastatic Breast Cancer (MK-7962-012)
  “administrative reasons (slow patient enrollment)” (61% 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.