Autopsy report · NCT00202371
Transfusion Effects in Myelodysplastic Patients: Limiting Exposure
Cause of deathSlow enrollment
“Too few inclusions”
Life of this trial
- Withdrawn before it enrolled anyone. Its dates are the sponsor's plans, not events that happened.
Vital statistics
- Status
- Withdrawn
- Phase
- Phase 4
- Sponsor
- Sanquin Research & Blood Bank Divisions
- Sponsor type
- University, hospital or other
- Conditions
- Myelodysplastic Syndromes
- Interventions
- Red Blood Cell transfusion
- Participants
- 0
- Sites
- 1
- Countries
- Netherlands
Trials that died the same way
- Pronostic Value of Endothelial Dysfunction in Heart Failure
“Not enough inclusions” - Bedside Therapeutic Monitoring of β-Lactam Levels in Newborns, Children and Adolescents Admitted to Intensive Care.
“insufficient inclusions” - Development of a Predictive Score for Local Complications of Femoral Bifurcation Surgery
“lack of inclusions” - A Lexico-semantic Program on Tactile Tablet for Patients With Alzheimer's Disease
“Lack of inclusion” - Impact of Anti-cytomegalovirus Treatment in the Management of Relapsing Ulcerative Colitis Requiring Vedolizumab Therapy
“low of inclusions”
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.