Clinical trial · Observational
Quantification of the Time and Effort Required for Peripheral Blood Stem Cell Collection -The European Perspective
Quantification of the Time and Effort Required for Peripheral Blood Stem Cell Collection - The European Perspective
NCT02287012CI-TRIAL-00024198completedClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This study aims to observe the effects of the availability of plerixafor on the time and effort associated with autologous peripheral blood stem cell collection.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Lymphoma | Lymphoma | ONTOLOGY_EXACT | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Time/Motion evaluation of actual apheresis | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- label
- Pre-Plerixafor era
- description
- The first era (Pre-Plerixafor era) will be defined as a two year period immediately preceding commercialization of plerixafor in Europe, (e.g., June 1, 2007 through June 1, 2009).
- label
- Plerixafor era
- description
- The second era (Plerixafor era) will be defined as July 1, 2010 through July 1, 2012).
- interventionNames
- Other: Time/Motion evaluation of actual apheresis
Primary outcomes (2)
- measure
- Type, duration and length of administration of mobilizing agents
- timeFrame
- one week
- description
- Number of visits for administration of mobilizing agents Duration (days) of administration of mobilizing agents Type of agents used as mobilizing agents
- measure
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: Patients must satisfy the following for the part 1 * Oncology patients diagnosed with Non-Hodgkin lymphoma who are candidates for autologous hematopoietic stem cell transplantation (HSCT) * A patient that fails to achieve a target CD34+\>20 cells/µl, before or on the first day of apheresis * Age \> 18 years Exclusion Criteria for the part 1 Patients with: * Age \< 18 years; * Primary diagnosis other than Non-Hodgkin lymphoma * Undergone prior autologous hematopoietic stem cell transplantation (HSCT)
References
Publications (0)
Data not yet available
No reference posted for this study.