Autopsy report · NCT05895253

Safety and Efficacy of Vibro-tactile Feedback for Patients Who Underwent Lower Limb Amputation

“recruitment rate of patients was not sufficient during COVID-19; problems with the quality of the primary outcome data collected”

The sponsor’s own words in the registry.

Life of this trial

• Registered 1 year 7 months after it had already started.
• Ran for about 6 months before it stopped.
• 18 participants enrolled.
• No results are posted on the registry.

Vital statistics

Status

Terminated

Phase

Na

Sponsor

Ludwig Boltzmann Institute for Traumatology - The research center in cooperation with AUVA

Sponsor type

Government (non-US federal)

Conditions

Amputation of Lower Limb Below Knee; Unilateral

Interventions

vibrotactile ground-contact feedback

Participants

18

Sites

1

Countries

Austria

Trials that died the same way

• A Study of Orally Administered JBPOS0101 in Refractory Infantile Spasms Patients
  “Difficulty with patient recruitment due to COVID-19” (84% match in meaning)
• Study Assessing Vagus Nerve Stimulation in CoViD-19 Respiratory Symptoms
  “A total of 21 patients were enrolled in the study resulting in 97 total collected specimen time points. Patient recruitment was halted due to greatly decreased numbers of patient hospitalizations for Covid-19.” (81% match in meaning)
• Iron Isomaltoside Compared With Iron Sucrosein Peritoneal Dialysis Patients
  “Difficult patient recruitment due to COVID-19 epidemic” (81% match in meaning)
• Effect of Anticoagulation Therapy on Clinical Outcomes in COVID-19
  “Due to lower COVID-19 cases and therefore difficulties with the recruitment.” (78% match in meaning)
• Treating Stimulant Addiction With Repetitive Transcranial Magnetic Stimulation
  “COVID-19 pandemic adversely affected recruitment.” (76% 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.