Probability of Chronic ICU-related pain in sepsis survivors

Probability of Chronic ICU-related pain in sepsis survivors - CIRPSS

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00033154

Enrollment

200

Registered

2023-12-01

Start date

2024-01-01

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

Sepsis, pain, sensory dysfunction, chronic intensive-care related pain

Interventions

Group 1: Exploration of sepsis survivors shortly after ICU/IMC discharge, where they were treated for at least five days

Eligibility

Sex/Gender

All

Age

18 Years to 85 Years

Inclusion criteria

Inclusion criteria: - ICU >5d - fluent in German - informed consent

Exclusion criteria

Exclusion criteria: - unable to give consent - Diagnosis of dementia, cognitive impairment, CNS damage

Design outcomes

Primary

Measure	Time frame
Probability of Chronic ICU-Related Pain (CIRP) in sepsis survivors with sensory dysfunction after ICU/IMC treatment	—

Secondary

Measure	Time frame
1. Prevalence of Chronic ICU-Related Pain (CIRP) in sepsis survivors without sensory dysfunction after ICU/IMC treatment 2. Prevalence of ICU acquired weakness in in sepsis survivors 3. Biomarker analysis for the prediction of CIRP	—

Countries

Germany

Contacts

Public ContactBeatrice Oehler

Universitätsklinikum Heidelberg

Beatrice.Oehler@med.uni-heidelberg.de+4962215634953

Outcome results

None listed

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