Autopsy report · NCT05735847

Surgery Induced Trauma After Total Versus Medial Unicompartmental Knee Arthroplasty (SITA)

“The study was terminated due to poor participant accrual. Recruitment was limited by competing clinical studies at the participating site, and the resources required to prolong the recruitment period were not available.”

The sponsor’s own words in the registry.

Life of this trial

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

Vital statistics

Status

Terminated

Sponsor

Hvidovre University Hospital

Sponsor type

University, hospital or other

Conditions

Knee Osteoarthritis; Arthritis; Surgery; Total Knee Arthroplasty; Unicompartmental Knee Arthroplasty

Interventions

Total Knee Arthroplasty (TKA); Unicompartmental Knee Arthroplasty (UKA)

Participants

29

Sites

1

Countries

Denmark

Trials that died the same way

• Dose-finding Study of MCI-196
  “This study has been terminated because of insufficient patient recruitment.” (85% match in meaning)
• Metformin and Transient Hyperglycemia
  “The research project was terminated due to lower than projected patient recruitment within the period of time allowed for the study.” (84% match in meaning)
• Comparison of the Live Birth Rate Between the PPOS and the GnRH Antagonist Protocol in Patients Undergoing IVF
  “The study was terminated due to difficulty in recruiting patients.” (83% match in meaning)
• A Study of Herceptin (Trastuzumab) in Patients With Metastatic or Advanced Gastric Cancer With Disease Progression
  “Study terminated due to slow patient recruitment.” (83% match in meaning)
• ADP-A2M4CD8 in HLA-A2+ Subjects With MAGE-A4 Positive Esophageal or Esophagogastric Junction Cancers (SURPASS-2)
  “Study was terminated due to difficulty recruiting subjects and lack of efficacy” (82% 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.