ClinicalTrials.gg
CompletedNCT07842562Updated Sep 25, 2026

Continuous Renal Replacement Therapy Circuit Lifespan in Intensive Care Patients

An observational study in Critical Illness and Acute Kidney Injury, sponsored by Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-25.

Primary conditionAcute Kidney InjuryRegistry: Critical IllnessReclassifiedWhy we changed it
Registry
Critical Illness — the first condition term the registry derived for this study.
ClinicalTrials.gg
Acute Kidney Injury
Why
  1. Critical Illness is a broad heading, used only when no more specific condition is named.
  2. The study's listed conditions name Acute Kidney Injury.
Confidence
High: the new condition is named in the study's own listed conditions. Of 351 hand-checked studies reclassified this way, 68% were exactly right and 84% in the right disease family; the registry's first term was right for 5% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital · Observational

Updated Sep 25, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
162
Ages
18 Years and older
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 90 studies in Acute Kidney Injury with a site in Turkey — 22 open to participants now, 23 under way, none of them phase 3. Acute Kidney Injury · Turkey.

Enrollment
27th of 73
162 · median 130
Started
2026
with 17 others
Observational
73 of 90
16 open now
Registered
84th of 90
by date

Among the 90 studies in Acute Kidney Injury with a site in Turkey, this one is the 27th largest by enrollment of the 73 observational ones that give a count, is one of 18 that started in 2026, is one of 73 observational ones, and was the 84th registered.

Acute Kidney Injury

1,691 studies on the registry are indexed under Acute Kidney Injury; 394 are open to participants now.

Browse Acute Kidney Injury studies →

Open to participants now

22 of the 90 studies in Acute Kidney Injury with a site in Turkey are open now. Recruiting first, the newest first:

17 more — sign in →

All 22 open studies →

A study can be open while its sites in Turkey have not opened yet or have stopped. Only those recruiting at a site in Turkey →

Who these studies take

Of the 230 Acute Kidney Injury studies recruiting now, 161 (70%) set no upper age limit and 36 (16%) stop at 75 or younger; 22 take children under 18; 25 take healthy volunteers.

This study: 18 Years and older · all sexes · no healthy volunteers.

The full table on the hub →

This tab as a report to print or save as PDF → With an account.

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Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 90 studies in Acute Kidney Injury with a site in Turkey, or all of them as a file.
02

Study summary

The goal of this retrospective observational study is to evaluate how long continuous renal replacement therapy (CRRT) circuits remain in use in adult intensive care unit patients and to describe how CRRT pressure measurements change over time. The main questions it aims to answer are:

Are higher maximum and mean transmembrane pressure (TMP) values associated with longer CRRT circuit lifespan? Do time-normalized pressure trajectories and cumulative TMP burden differ between circuits with different lifespans? Do access pressure patterns influence the relationship between pressure measurements and circuit lifespan? Researchers will analyze archived CRRT device log files, including access pressure, filter pressure, effluent pressure, return pressure, and TMP measurements. No additional procedures, interventions, or study visits will be required. No directly identifiable patient information will be included in the analytical dataset.

03

Conditions studied

  • Critical Illness
  • Acute Kidney Injury

Browse trials for

Keywords

  • Continuous Renal Replacement Therapy
  • Continuous Kidney Replacement Therapy
  • CRRT Circuit Lifespan
  • Transmembrane Pressure
  • Circuit Pressure Dynamics
04

In context

Acute Kidney Injury Reclassified

1,691 studies on the registry are indexed under Acute Kidney Injury; 394 are open to participants now.

This study's enrollment of 162 is close to the median of 160 across 814 observational studies indexed under Acute Kidney Injury.

Browse Acute Kidney Injury studies →

Lead sponsor

Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital is the lead sponsor of 75 studies on the registry; 18 are open to participants now.

Compared within Acute Kidney Injury, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Critical Illness. The counts are of registry records indexed under each term, refreshed daily. How we classify →

05

Who can participate

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

Study population

The study population consists of adult intensive care unit (ICU) patients who underwent continuous renal replacement therapy (CRRT) using the Prismaflex platform. Archived device log files (LOX format) generated during routine clinical care were evaluated. The unit of analysis was the individual CRRT session rather than the patient, as device logs were structured at the treatment-session level and patient-level linkage was not consistently available. Eligible sessions had a minimum runtime of 1 hour and at least 60 valid, chronologically ordered pressure recordings.

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

  • Archived CRRT treatment sessions performed in adult intensive care unit patients.
  • CRRT sessions recorded on the Prismaflex platform and available as LOX device log files.
  • Sessions with a circuit lifespan of at least 1 hour, defined as the time between the first and last valid pressure recording.
  • Sessions containing sufficient time-stamped pressure data for analysis, including at least 60 valid pressure measurements.
  • Sessions with available pressure recordings for the relevant variables, including transmembrane pressure, access pressure, filter pressure, effluent pressure, and/or return pressure.
  • Sessions with adequate data integrity and chronologically interpretable pressure records.

Exclusion criteria

Exclusion Criteria:

  • CRRT sessions with a runtime of less than 1 hour.
  • Sessions with missing pressure tables.
  • Sessions with fewer than 60 pressure measurements.
  • Sessions with missing or incomplete primary device records.
  • Sessions with missing timestamps or pressure records that cannot be ordered chronologically.
  • Sessions with inadequate pressure-data density for trajectory analysis.
  • Sessions with major data-integrity problems that prevent reliable calculation of circuit lifespan or pressure-derived variables.
  • Duplicate or otherwise unusable device-log records.
06

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
162 participants (actual)
Patient registry
No

Groups and cohorts

  • CRRT Circuit Lifespan <12 Hours

    CRRT sessions with a circuit lifespan of less than 12 hours, defined as the time between the first and last valid pressure recording in the device log. No intervention was assigned.

    Other: Archived CRRT Device Log Data

  • CRRT Circuit Lifespan 12 to <24 Hours

    CRRT sessions with a circuit lifespan of at least 12 hours but less than 24 hours, defined as the time between the first and last valid pressure recording in the device log. No intervention was assigned.

    Other: Archived CRRT Device Log Data

  • CRRT Circuit Lifespan 24 to <48 Hours

    CRRT sessions with a circuit lifespan of at least 24 hours but less than 48 hours, defined as the time between the first and last valid pressure recording in the device log. No intervention was assigned.

    Other: Archived CRRT Device Log Data

  • CRRT Circuit Lifespan ≥48 Hours

    CRRT sessions with a circuit lifespan of 48 hours or longer, defined as the time between the first and last valid pressure recording in the device log. No intervention was assigned.

    Other: Archived CRRT Device Log Data

Interventions

  • OtherArchived CRRT Device Log Data

    This observational study involves no assigned intervention, treatment, device use, or change in clinical care. The study analyzes archived pressure recordings from CRRT device log files generated during routine clinical care. The analyzed variables include access pressure, filter pressure, effluent pressure, return pressure, and transmembrane pressure. CRRT circuit lifespan is evaluated retrospectively according to the time between the first and last valid pressure recording. No additional procedures or study-related interventions are performed.

07

What researchers measure

Primary outcomes

  1. Maximum Transmembrane Pressure Across CRRT Circuit Lifespan Categories

    To compare maximum transmembrane pressure values among CRRT sessions grouped by circuit lifespan: less than 12 hours, 12 to less than 24 hours, 24 to less than 48 hours, and 48 hours or longer.

    Time frame: From the first to the last valid pressure recording of each CRRT session

Secondary outcomes

  1. Initial 6-hour TMP slope

    The initial 6-hour transmembrane pressure (TMP) slope will be calculated from the time-stamped TMP measurements obtained during the first 6 hours of each CRRT session. It will be expressed in mmHg per hour and will be evaluated as a secondary pressure-dynamics measure in relation to CRRT circuit lifespan and lifespan categories. Sessions without sufficient pressure data during the initial 6-hour period will be excluded from this specific analysis.

    Time frame: During the first 6 hours of each CRRT session

08

Study locations

1 site
  • Dr. Abdurrahman Yurtaslan Ankara Oncology Hospital
    Yenimahalle, Ankara 06200, Turkey (Türkiye)
09

References and documents

Individual participant data

Plan to share: No — Individual participant data will not be shared with other researchers. This retrospective study uses archived CRRT device log files, and patient-level linkage was not consistently available. The analytical dataset does not include directly identifiable patient information; however, the underlying device logs and study dataset will not be made publicly available because of institutional data-protection requirements and the terms of the ethics approval. Aggregate results will be reported in the publication.

No publications or documents are linked to this record.

10

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Sep 2026 to primary completion in Sep 2026, 0 months.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 21, 2026
First posted
Sep 25, 2026
StartActual
Sep 20, 2026
Primary completionActual
Sep 20, 2026
CompletionActual
Sep 21, 2026
Last update
Sep 25, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Sep 25, 2026
Show all 1 update
  1. Sep 25, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

11

Registry details

Key details

Study ID
NCT07842562
Lead sponsor
Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital
Responsible party
Arif Timuroğlu, MD (anesthesiology specialist, M.D., Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital) — Principal investigator
First posted
Sep 25, 2026
Start date
Sep 20, 2026
Primary completion
Sep 20, 2026
Completion
Sep 21, 2026
Last update
Sep 25, 2026

Oversight

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

Not currently enrolling

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

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