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Protocolized Reduction of Non-resuscitation Fluids Versus Usual Care in Septic Shock Patients

Study acronym: REDUSE
StatusRecruiting
PhaseNot applicable
Started2023-11-27
View on ClinicalTrials.gov ↗

Amendment history

2026-03-26
Study Status, Contacts/Locations v14
Study sitesdetails revised at 2 of 22 sites
2026-02-18
Study Status, Contacts/Locations v13
Study sites20→22
2025-12-08
Study Status, Contacts/Locations v12
Study sites19→20
2025-11-19
Study Status, Contacts/Locations v11
Study sitesdetails revised at 1 of 19 sites
2025-11-17
Study Status, Contacts/Locations v10
Study sites17→19
Show 9 earlier versions
2025-09-23
Study Status, Contacts/Locations v9
Study sites12→17
2025-01-30
Study Status, Contacts/Locations v8
Study sites13→12
2024-12-16
Study Status, Contacts/Locations v7
Study sitesdetails revised at 1 of 13 sites
2024-12-11
Study Status, Oversight, Contacts/Locations v6
Study sitesdetails revised at 1 of 13 sites
2024-11-11
Study Status, Oversight, Contacts/Locations v5
Study sitesdetails revised at 2 of 13 sites
2024-11-04
Study Status, Contacts/Locations v4
Study sites9→13
2024-04-08
Study Status, Outcome Measures, Contacts/Locations v3
Study sites6→9
Secondary endpoints4 entries, revised
DaysMechanical alive and ventilation-free of mechanical ventilationdays
2024-02-28
Not Yet Recruiting→Recruiting Study Status, Contacts/Locations v2
Trial statusNot Yet Recruiting→Recruiting
Start dateestimated 2024-01-01→confirmed 2023-11-27
Study sitesdetails revised at 6 of 6 sites
2023-11-30
Study Status, Outcome Measures v1
Re-verified, no change to tracked fields
2023-11-14
Original filing
Region Skane
146 trials monitored
See 5 trials at risk
The objective of this trial is to assess the beneficial and harmful effects of a restrictive strategy for administration of non-resuscitation fluids in adult patients with septic shock.
Trial Details
NCT Number NCT06140147
Lead Sponsor Region Skane
Conditions Septic Shock
Enrollment 1,850 participants
Start Date 2023-11-27
Primary Completion 2027-12-31 (estimated)
Study Completion 2028-07-01 (estimated)
Updated on ClinicalTrials.gov 2026-09-18