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WithdrawnNCT06134245HOUSEUpdated Sep 11, 2026

HOme USability Evaluation

An observational study in Cancer, sponsored by Entia Ltd. Withdrawn. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-11.

Sponsored by Entia Ltd · Observational

Why this study was withdrawn
Change in trial pipeline. Study no longer required.
Study type
Observational
Model
Case-only
Time perspective
Cross-sectional
Enrollment
0
Ages
18 Years and older
Sex
All
01

Study summary

To validate the usability and safety of the Liberty Analyser.

02

Conditions studied

  • Cancer

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03

In context

Neoplasms

9,365 studies on the registry are indexed under Neoplasms; 2,489 are open to participants now.

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Lead sponsor

Entia Ltd is the lead sponsor of 16 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Adults with a diagnosis of solid tumour cancer, who are currently undergoing systemic anti-cancer therapy

Inclusion criteria

  • Undergoing systemic anti-cancer therapy (SACT)
  • Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0, 1, 2 at enrolment
  • Adequate English language skills (not requiring a translator) to participate in participant training and use the Entia Liberty analyser
  • Patients capable of providing written informed consent

Exclusion criteria

Exclusion Criteria:

  • History or current diagnosis of haematological malignancy
  • Patients with eyesight or hearing limitations or other disabilities that preclude the use of the Entia Liberty analyser or participation in training
  • Inadequate use and understanding of the English language, requiring a translator
05

Study design

Observational model
Case-only
Time perspective
Cross-sectional
Enrollment
0 participants (actual)
Patient registry
No

Interventions

  • DeviceEntia Liberty

    Home monitoring

06

What researchers measure

Primary outcomes

  1. The Entia Liberty Analyser is easy to use

    Users can easily carry out a test using the Entia Liberty Analyser

    Time frame: Through study completion, 1 day

  2. The Entia Liberty Analyser is safe to use

    Results obtained using the Entia Liberty Analyser are valid and reliable

    Time frame: Through study completion, 1 day

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 11, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06134245
Lead sponsor
Entia Ltd
Responsible party
Sponsor
First posted
Nov 18, 2023
Start date
Mar 1, 2024 (estimated)
Primary completion
Jun 30, 2024 (estimated)
Completion
Jun 30, 2024 (estimated)
Last update
Sep 11, 2026

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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Discussion

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