ClinicalTrials.gg
WithdrawnNCT05260099Updated Dec 20, 2022

Remove LPS Registry

An observational study in Suspected or Diagnosed Endotoxemia Casued by Gram-negative Bacteria, sponsored by Alteco Medical AB. Withdrawn. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2022-12-20.

Sponsored by Alteco Medical AB · Observational

Why this study was withdrawn
Company decision not to start study
Study type
Observational
Model
Other
Time perspective
Other
Enrollment
0
Ages
18 Years and older
Sex
All
01

Study summary

This registry will collect and validate regulatory-grade real-world data (RWD) on the usage of the LPS-Adsorber and the outcomes from using the LPS-Adsorber in various patient populations (various sub-registries) that also have suspected endotoxemia. This data can be then used in real-world evidence (RWE) generation. It will also create reusable infrastructure to allow creation or affiliation with many additional RWD/RWE efforts both prospective and retrospective in nature.

02

Conditions studied

  • Suspected or Diagnosed Endotoxemia Casued by Gram-negative Bacteria

Browse trials for

03

In context

Endotoxemia

81 studies on the registry are indexed under Endotoxemia; 7 are open to participants now.

Browse Endotoxemia studies →

Lead sponsor

Alteco Medical AB is the lead sponsor of 2 studies on the registry; none are 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

Patients with suspected or diagnosed sepsis caused by gram-negative bacteria.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Weight > 30 kilos

Specific sub-registry criteria are possible.

Exclusion criteria

Exclusion Criteria:

  • None
05

Study design

Observational model
Other
Time perspective
Other
Enrollment
0 participants (actual)
Target follow-up
30 Days
Patient registry
Yes

Groups and cohorts

  • Retrospective

    Patients not treated with LPS Adsorber

  • Prospective

    Patients treated with LPS Adsorber

    Device: LPS Adsorber

Interventions

  • DeviceLPS Adsorber

    LPS Adsorber, binding endotoxin caused by suspected or verified gram-negative bacteria.

06

What researchers measure

Primary outcomes

  1. The primary endpoint will be the time needed to achieve patient stabilization from the time of treatment.

    Time frame: 30 days

Secondary outcomes

  1. Secondary Outcomes will be to document the change in a patient's symptoms of infection over time.

    Time frame: 30 days

  2. Rate of complaints and incidents related to the medical device during the whole registry.

    Time frame: 30 days

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No

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 Dec 20, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05260099
Lead sponsor
Alteco Medical AB
Responsible party
Sponsor
First posted
Mar 2, 2022
Start date
Nov 2022 (estimated)
Primary completion
Nov 2022 (estimated)
Completion
Jul 2023 (estimated)
Last update
Dec 20, 2022

Oversight

Data monitoring committee
No
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 Dec 2022. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion