Autopsy report · NCT02489175

Stomaplasty Ring (KoringTM) for Prevention of Parastomal Hernia

“The device used was removed from the market”

The sponsor’s own words in the registry.

Life of this trial

• Ran for about 3 months before it stopped.
• 4 participants enrolled.
• No results are posted on the registry.

Vital statistics

Status

Terminated

Phase

Na

Sponsor

Nicolas DEMARTINES

Sponsor type

University, hospital or other

Conditions

Parastomal Hernia

Interventions

Stomaplasty KoringTM

Participants

4

Sites

7

Countries

Switzerland

Trials that died the same way

• A Study of Renal Denervation in Patients With Treatment Resistant Hypertension
  “Manufacturer updated device technology.” (62% match in meaning)
• Radiographic Analysis Using PureGen Versus Autologous Bone in Posterolateral Fusion (PLF)
  “Product no longer on the market” (61% match in meaning)
• Care China-Diabetes
  “the product was delisted.” (60% match in meaning)
• Active Surveillance Post-Approval Atudy of the Stelkast Surpass Acetabular System
  “Product is no longer being manufactured and marketed.” (57% match in meaning)
• Xenon-anesthesia on Patients Undergoing Major Liver-resection
  “A device would have had to be maintained. The maintenance company is insolvent; both another maintenance company and another serviced device were not available.” (56% 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.