Autopsy report · NCT05830149

Safety and Treatment of Cryoinsufflation in Treatment of Hidradenitis Suppurativa

“Did not have staffing to support the study”

The sponsor’s own words in the registry.

Life of this trial

• Registered 3 years 11 months after it had already started.
• Ran for about 2 months before it stopped.
• 1 participant enrolled.
• No results are posted on the registry.

Vital statistics

Status

Terminated

Phase

Na

Sponsor

Henry Ford Health System

Sponsor type

University, hospital or other

Conditions

Hidradenitis Suppurativa

Interventions

Cryoinsufflation; Deroofing

Participants

1

Sites

1

Countries

United States

Trials that died the same way

• Midodrine Use in Septic Shock
  “No funding for the study; not enough staff” (76% match in meaning)
• 24-hour IOP Fluctuation Profile Recorded With SENSIMED Triggerfish in Primary Open-angle Glaucoma (POAG) Patients After Cataract Surgery
  “Due to staff departures we were unable to execute this study” (76% match in meaning)
• Analgesic Efficacy of Intravenous Lidocaine for Postoperative Pain Following Adult Spine Surgery
  “Did not have the research staff necessary to follow through with this study.” (76% match in meaning)
• Mindful Yoga Therapy as an Adjunctive Treatment for PTSD Among OEF/OIF Veterans
  “Did not have funding or resources to carry out study” (75% match in meaning)
• Whole Body Vibration for OSA
  “Study was not funded, and therefore not conducted” (74% 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.