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Trial · NCT05163405

Perspectives of Subcutaneous Velcade at Home of Patients With Myeloma.

NCT05163405, Completed, Karin B. Ø. Dieperink

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Perspectives of Subcutaneous Velcade at Home of Patients With Myeloma. Trials, record NCT05163405. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT05163405

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Perspectives of Subcutaneous Velcade at Home of Patients With Myeloma.
NCT number
NCT05163405
Status
Completed
Enrollment
10 participants, actual
Lead sponsor
Karin B. Ø. Dieperink
Conditions
Multiple Myeloma
Interventions
Bortezomib
First posted
2021-12-20
Last updated
2025-08-22

Source ClinicalTrials.gov

Registered outcomes4

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryPatients experience of self-administration of VelcadeThrough study completion, from 01. dec. 2019 until 01. jun. 2022Qualitative interviews with all 10 included patients
SecondaryOrganizational perspectiveThrough study completion, from 01. dec. 2019 until 01. jun. 2022Patients and health professionals (including pharmacy staff) registration of time spend on treatment on all 10 included patients.
SecondaryHealth care perspectiveThrough study completion, from 01. dec. 2019 until 01. jun. 2022Focus group interview with healthcare professionals involved in the treatment.
SecondaryFinancial perspectiveThrough study completion, from 01. dec. 2019 until 01. jun. 2022Evaluation of financial savings on home treatment including healthcare salaries and transportation.

Outcomes0

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.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

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/NCT05163405

GET https://conductscience.org/api/trials/v1/NCT05163405/registered