Trial · NCT06581055
A Retrospective Study to Describe Real-World Treatment Patterns and Clinical Outcomes Among Patients With Myelodysplastic Syndromes
NCT06581055, Withdrawn, Bristol-Myers Squibb
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. A Retrospective Study to Describe Real-World Treatment Patterns and Clinical Outcomes Among Patients With Myelodysplastic Syndromes. Trials, record NCT06581055. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06581055
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- A Retrospective Study to Describe Real-World Treatment Patterns and Clinical Outcomes Among Patients With Myelodysplastic Syndromes
- NCT number
- NCT06581055
- Status
- Withdrawn
- Enrollment
- 0 participants, actual
- Lead sponsor
- Bristol-Myers Squibb
- Conditions
- Myelodysplastic Syndromes (MDS)
- Interventions
- Luspatercept, Epoetin Alfa
- First posted
- 2024-08-30
- Last updated
- 2024-10-09
Source ClinicalTrials.gov
Registered outcomes18
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Participant treatment patterns: Type of treatment received | Up to 24 months | |
| Primary | Participant treatment patterns: Duration of treatment received | Up to 24 months | |
| Primary | Participant treatment patterns: Dosage of treatment received | Up to 24 months | |
| Primary | Participant treatment patterns: Dosing route of treatment administration | Up to 24 months | |
| Primary | Participant treatment patterns: Reason for treatment administration | Up to 24 months | |
| Primary | Participant treatment patterns: Time to next line of therapy (LoT) | Up to 24 months | |
| Primary | Participant treatment patterns: Reason for treatment discontinuation | Up to 24 months | |
| Primary | Participant treatment patterns: Type of concomitant medications received | Up to 24 months | |
| Primary | Participant treatment patterns: Start and end dates of concomitant medications received | Up to 24 months | |
| Secondary | Participant clinical outcomes: Number of units of red blood cell transfusions received | Up to 24 months |
1 to 10 of 18Source ClinicalTrials.gov
See all 18 registered outcomesOutcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT06581055
GET https://conductscience.org/api/trials/v1/NCT06581055/registered