Rhabdomyolysis in Sepsis: a prospective observational study

Rhabdomyolysis in Sepsis: a prospective observational study - RM-Sepsis

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00034799

Enrollment

125

Registered

2024-08-06

Start date

2024-09-02

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

A41.9

Interventions

Group 1: All patients who are treated with sepsis (according to Sepsis 3 definition) in the medical intensive care unit

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: All patients who are treated with sepsis (according to Sepsis 3 definition) in the medical intensive care unit

Exclusion criteria

Exclusion criteria: Refusal to use the data collected Age < 18 years Women during pregnancy and breastfeeding

Design outcomes

Primary

Measure	Time frame
ICU-mortality of septic patients depending on additional rhabdomyolysis	—

Secondary

Measure	Time frame
90-day mortality Hospital mortality ICU-length of stay Creatinine kinetics daily diuresis AKIN stage at diagnosis and over time Need for renal replacement therapy Dialysis duration and dialysis procedure Creatinine value at discharge eGFR and CKD stage at discharge Dialysis dependency at discharge	—

Countries

Germany

Contacts

Public ContactLorenz Weidhase

Universitätsklinikum Leipzig, Interdisziplinäre Internistische Intensivmedizin

lorenz.weidhase@medizin.uni-leipzig.de+49 341 9712705

Outcome results

None listed

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