Autopsy report · NCT05891002
Accuracy of Robotically Assisted Cranial Biopsies
Cause of deathSafety, also staffing, sites or logistics
“The clinical study could not be commenced due to the Principal Investigator's limited availability, which has significantly impacted the feasibility of continuing the study as planned. No safety concerns or adverse events were detected.”
Life of this trial
- Registered 5 months before it started.
- Ran for about 1 year 9 months before it stopped.
- 4 participants enrolled.
- Results were posted on the registry 10 months after it ended.
Vital statistics
- Status
- Terminated
- Sponsor
- Brainlab AG
- Sponsor type
- Industry
- Conditions
- Intracranial Neoplasm
- Interventions
- Cirq® Robotic Alignment Module Cranial
- Participants
- 4
- Sites
- 1
- Countries
- France
Trials that died the same way
- The Effect of Continued Mechanical Ventilation on the Occurrence of Myocardial Ischemia
“After the passing of the principal investigator, the clinical trial could not be continued.” - An Efficacy and Safety Study of JNJ-26113100 in the Treatment of Adult Atopic Dermatitis
“The study was stopped due to a non-clinical safety finding.” - Efficacy of Traumatic Memory Modification Using Memory Reconsolidation and Propranolol Among Adolescents With PTSD
“The study could not begin within the period of validity of the authorizations. The project has been abandoned in its initially authorized form. The final study report will not be produced.” - A Dose-finding Study of Birabresib (MK-8628) in Participants With Recurrent Glioblastoma Multiforme (MK-8628-002)
“This study was terminated due to lack of clinical activity and not due to safety reasons.” - A Study of Isatuximab-based Therapy in Participants With Lymphoma
“Study was stopped after interim analysis for all 4 cohorts with results either not fulfilling the pre-planned interim analysis criteria or fulfilling the criteria but as per sponsor decision. It was not due to any safety concern”
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.