Autopsy report · NCT00959738
Diverting Loop Ileostomy: With or Without Rod
Cause of deathFutility, also regulatory or ethics
“Difference found in interim analysis, not ethical to continue”
Life of this trial
- Registered 1 year after it had already started.
- Ran for about 6 years 3 months before it stopped.
- 121 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Na
- Sponsor
- Insel Gruppe AG, University Hospital Bern
- Sponsor type
- University, hospital or other
- Conditions
- Ileostomy; Rectal Neoplasms
- Interventions
- Diverting loop ileostomy with rod; diverting loop ileostomy without rod
- Participants
- 121
- Sites
- 1
- Countries
- Switzerland
Trials that died the same way
- Moxonidine in Patients Undergoing Vascular Surgery
“Study was stopped after pre-definied interim analysis because of no effects” - ICVT in HPV-induced Genital Lesions of Immunocompromised and Immunocompetent Patients
“Lack of effect in interim analysis” - Linifanib in Treating Patients With Advanced, Refractory Colorectal Cancer
“Interim analysis determined the study did not meet criteria to proceed” - Conversational Hypnosis in Women Undergoing Imaging for Breast Cancer
“Results not achievable after interim analysis conclusions and recruting difficulty” - 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.”
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.