Acute Kidney Injury and Intermittent Dialysis Dose
NCT07924137, Not yet recruiting, Assistance Publique - Hôpitaux de Paris
Trial 9
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Acute Kidney Injury and Intermittent Dialysis Dose | ClinicalTrials.gov |
| NCT number | NCT07924137 | ClinicalTrials.gov |
| Status | Not yet recruiting | ClinicalTrials.gov |
| Enrollment | 200 participants, estimated | ClinicalTrials.gov |
| Lead sponsor | Assistance Publique - Hôpitaux de Paris | ClinicalTrials.gov |
| Conditions | Acute Kidney Injury, Renal Dialysis, Renal Replacement Therapy, Critical Illness, Intensive Care (ICU) | ClinicalTrials.gov |
| Interventions | Intermittent hemodialysis (no study-assigned intervention) | ClinicalTrials.gov |
| First posted | 2026-11-09 | ClinicalTrials.gov |
| Last updated | 2026-11-09 | ClinicalTrials.gov |
Registered outcomes 23
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Kt: volume of blood totally cleared of urea during the session (L) | Up to 30 days | Quantitative value of each dialysis dose parameter, measured at each dialysis session | ClinicalTrials.gov |
| Primary | Kt/Vd: Kt divided by the patient's urea distribution volume (Vd, L) | Up to 30 days | Quantitative value of each dialysis dose parameter, measured at each dialysis session | ClinicalTrials.gov |
| Primary | Double-pool Kt/Vd: Kt/Vd calculated with a double-pool urea kinetic model | Up to 30 days | Quantitative value of each dialysis dose parameter, measured at each dialysis session | ClinicalTrials.gov |
| Primary | URR: urea reduction ratio, based on post-dialysis plasma urea | Up to 30 days | Quantitative value of each dialysis dose parameter, measured at each dialysis session | ClinicalTrials.gov |
| Primary | SRI: solute removal index, based on urea in the effluent | Up to 30 days | Quantitative value of each dialysis dose parameter, measured at each dialysis session | ClinicalTrials.gov |
| Secondary | Death or dialysis dependence | Up to day 29 | Binary variable: death or dialysis dependence before Day 29 after inclusion. | ClinicalTrials.gov |
| Secondary | Renal recovery | Up to day 29 | Defined by a glomerular filtration rate ≥ 60 mL/min/1.73 m2 (KDIGO). | ClinicalTrials.gov |
| Secondary | CAM-ICU (Confusion Assessment Method for the ICU) | At inclusion | positive or negative for delirium | ClinicalTrials.gov |
| Secondary | CAM-ICU (Confusion Assessment Method for the ICU) | At day 3 | positive or negative for delirium | ClinicalTrials.gov |
| Secondary | CAM-ICU (Confusion Assessment Method for the ICU) | At day 6 | positive or negative for delirium | ClinicalTrials.gov |
| Secondary | CAM-ICU (Confusion Assessment Method for the ICU) | At day 29 | positive or negative for delirium | ClinicalTrials.gov |
| Secondary | Glasgow Coma Scale | At inclusion | varying to 3 to 15, higher scores indicating better consciousness | ClinicalTrials.gov |
| Secondary | Glasgow Coma Scale | At day 3 | varying to 3 to 15, higher scores indicating better consciousness | ClinicalTrials.gov |
| Secondary | Glasgow Coma Scale | At day 6 | varying to 3 to 15, higher scores indicating better consciousness | ClinicalTrials.gov |
| Secondary | Glasgow Coma Scale | At day 29 | varying to 3 to 15, higher scores indicating better consciousness | ClinicalTrials.gov |
| Secondary | RASS (Richmond Agitation-Sedation Scale) | At inclusion | -5 (unarousable) to +4 (combative), 0 meaning alert and calm. | ClinicalTrials.gov |
| Secondary | RASS (Richmond Agitation-Sedation Scale) | At day 3 | -5 (unarousable) to +4 (combative), 0 meaning alert and calm. | ClinicalTrials.gov |
| Secondary | RASS (Richmond Agitation-Sedation Scale) | At day 6 | -5 (unarousable) to +4 (combative), 0 meaning alert and calm. | ClinicalTrials.gov |
| Secondary | RASS (Richmond Agitation-Sedation Scale) | At day 29 | -5 (unarousable) to +4 (combative), 0 meaning alert and calm. | ClinicalTrials.gov |
| Secondary | Hemodynamic instability | Up to day 29 | During IHD sessions Defined as vascular filling and/or initiation or increase of a vasopressor and/or discontinuation or reduction of the ultrafiltration rate. | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
|---|
Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 0
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|
Grants 0
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.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years | Source |
|---|
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|
Source 5
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.4.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
| NIH clinical studies file | 2026-11-13 | ClinicalTrials.gov |
Release trials-2026-11-12-0.4.0
ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)