Clinical trial · Observational
Myeloma Treatment in Real Life
Myeloma Treatment in Real Life : Pharmacoepidemiological Approach in Midi-pyrénées
- 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)
As part of an oral treatment regimen in ambulatory practice, certain uses in connection with drug consumption associated could alter treatment outcomes observed in randomized clinical trials. The increase in progression-free survival in myeloma may be accompanied by an impaired quality of life and a resurgence of pain symptoms over time, which could potentially lead to medication overuse involving painkillers but also psychotropic drugs. These combined consumption may affect survival through mechanisms of pharmacological or non-pharmacological interactions. As part of this project, we wish to explore the scheme of adherence to myeloma drugs, and thus validate the decision diagram of hypothesis of not adequate of drug use in ambulatory conditions, from observational data. This discrepancy could result from poor adherence or suboptimal drug use but also from concomitant exposures to other drugs which may interact with myeloma. Before considering a study of greater magnitude that could address the consequences of non optimal drug use on clinical response criteria, such as duration of response or survival, it seems appropriate to confirm these assumptions within ' an exploratory study.
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 |
|---|---|---|---|
| Multiple Myeloma | Multiple Myeloma | CURATED_EXACT | 0.92 |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Administrative data | Other | — | UNRESOLVED |
| Drug exposition data | Other | — | UNRESOLVED |
| Medical data | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- label
- Patients with multiple myeloma
- description
- Data to be collected are : * Drug exposition data * Administrative data * Medical data
- interventionNames
- Other: Administrative data
- Other: Medical data
- Other: Drug exposition data
Primary outcomes (1)
- measure
- Evaluation of myeloma treatment observance in real life as assessed by data collected in french national system of information of health insurance
- timeFrame
- Through the end of study (15 months)
Secondary outcomes (3)
- measure
- Description deliverance scheme of treatment used in multiple myeloma as assessed by data collected in french national system of information of health insurance
- timeFrame
- Through the end of study (15 months)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Beneficiaries or entitled to health insurance or covered by the national system of information of health insurance * Identified as multiple myeloma * Incident patient : Subject presenting none of inclusion criteria during the 6 months observation period Exclusion Criteria: * Non incident patient : Subject presenting at least one of inclusion criteria during the 6 months observation period
References
Publications (0)
Data not yet available