Autopsy report · NCT06134661
Accelerated rTMS for Psychomotor Slowing
Cause of deathOther
“Planned interim analyses demonstrated that the main aim of the study was already met. Recruitment was stopped. Early termination was unrelated to safety.”
Life of this trial
- Registered 1 month after it had already started.
- Ran for about 11 months before it stopped.
- 25 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Na
- Sponsor
- University of Bern
- Sponsor type
- University, hospital or other
- Conditions
- Schizophrenia; Psychosis; Schizophrenia and Related Disorders; Schizo Affective Disorder; Brief Psychotic Disorder
- Interventions
- cTBS (continuous Theta Burst Stimulation)
- Participants
- 25
- Sites
- 1
- Countries
- Switzerland
Trials that died the same way
- Adherence to Antidepressant Treatment in Subjects With Depression
“The study was terminated early based on the planned interim analysis that did not meet criteria for continuation.” - Study of Vascular Function Before vs After Smoking an E-cigarette as Compared to a Normal Cigarette
“due to recruitment reasons the study was prematurely ended” - Paracetamol With Caffeine to Treat Episodic Tension Type Headache
“Study was terminated due to unforeseen difficulties with subject recruitment. No safety issues were identified in the study with this new formulation.” - 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” - A Study to Determine the Performance of the Press Fit Condylar (P.F.C.) Sigma RP-F Knee System
“Study was terminated early due to prolonged recruitment period.”
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.