Autopsy report · NCT02372695
Effect of Paricalcitol Over Vessel Wall
Cause of deathOther
“Protocol showed to be inappropriate for the evaluation of the selected patients”
Life of this trial
- Registered 8 months after it had already started.
- Ran for about 10 months before it stopped.
- 50 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Phase 4
- Sponsor
- Effice Servicios Para la Investigacion S.L.
- Sponsor type
- Industry
- Conditions
- Nephropathy
- Interventions
- Paricalcitol
- Participants
- 50
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“Per protocol, study was terminated due to low rate of randomized patients.” - Impact of Current Smoking in the Tolerance of Bronchoscopy
“the physician responsable for this protocol left our hospital” - Improving Medication Adherence in Post-ACS Patients
“This was a dosing study to determine acceptability. Participants found protocol burdensome and so we terminated.”
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.