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Proenkephalin as a guide to cessation of renal replacement therapy in the ICU: A single-center observational, prospective pilot study

Proenkephalin as a guide to cessation of renal replacement therapy in the ICU: A single-center observational, prospective pilot study - PROENK-Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00025981
Enrollment
200
Registered
2021-08-16
Start date
2023-06-14
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Kidney Injury on ICU

Interventions

Group 1: - Proenkephalin (POCT) and other markers at end of dialysis - Proenkephalin (POCT) and other markers at dialysis end + 72h - Proenkephalin (POCT) and other markers at dialysis end + 72h + 96h

Sponsors

Universitätsmedizin Göttingen
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: Critically Ill patients in ICU with CRRT

Exclusion criteria

Exclusion criteria: Age < 18, no informed consent, no CRRT

Design outcomes

Primary

MeasureTime frame
Measurement of proenkephalin during CRRT - weaning. Subsequently, check whether weaning was successful (Yes / No).

Countries

Germany

Contacts

Public ContactSteffen Dickel

Klinik für AnästhesiologieUniversitätsmedizin Göttingen

steffen.dickel@med.uni-goettingen.de+4955166045

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026