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What It's like to have sepsis and kidney damage: patients share their stories

NCT ID NCT07180238

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This completed study interviewed 28 people who had sepsis-associated acute kidney injury (SA-AKI) to learn about their symptoms, impacts, and treatment experiences. Participants shared their perspectives in 60-minute interviews. The goal was to better understand what patients go through, not to test a new treatment.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

28 people

The number who actually took part.

Started

May 2025

Finished

Sep 2025

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Adults who have experienced SA-AKI. A subset of the interviews (50%-70%) will include a caregiver/care-partner in a dyad interview (a type of interview that involves two respondents). In addition, the study team targets for a minimum of 50% of participants that have been diagnosed with SA-AKI no longer than 5 years ago.

Ages

18 to 85 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: Potential participants who were diagnosed with SA-AKI (KDIGO stage I, II or III) must meet the following eligibility criteria: * ≥18 to ≤ 85 years of age * First diagnosis of SA-AKI at least 6 months prior to screening date, but no more than 10 years * Admitted due to sepsis and/or AKI to intensive care unit (ICU), intermediate care unit (IMCU), or high-dependency care unit, or developed sepsis and/or AKI during their inpatient hospital stay. * Resident of country of study (US or Germany) * Access to computer, tablet, or smartphone with internet connection * Willing to participate in an audio recorded interview Participants will be required to present confirmation of diagnosis (COD) rather than relying on a self-reported diagnosis. Sepsis and AKI diagnoses will be confirmed through one of the following: * Copy of medical records (e.g., portable document format \[PDF\] file of electronic health record) * Physician confirmation of diagnosis of sepsis and AKI (post-sepsis) Potential caregiver participants must meet the following criteria: * ≥18 to ≤ 85 years of age * Primary caregiver/care-partner for eligible participant who experienced SA-AKI * Resident of country of study (US or Germany) * Access to computer, tablet, or smartphone with internet connection * Willing to participate in an audio recorded interview Exclusion Criteria: Potential participants are not eligible if they meet any of the following criteria: * Less than age of majority in locality (Participant is not considered an adult in their country or region) * Not willing to participate in an audio recorded interview * Not able to participate in the interview or complete required study surveys, based on the discretion of the study team

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Novartis Investigative Site

    East Hanover, New Jersey, 07936-1080, United States