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QuantiPEIT-Study: Quantification of pleural effusions by electrical impedance tomography

QuantiPEIT-Study: Quantification of pleural effusions by electrical impedance tomography - QuantiPEIT

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00033369
Enrollment
30
Registered
2024-01-18
Start date
2023-09-11
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

J90

Interventions

Group 1: Adult patients with pleural effusion under monitoring with electrical impedance tomography

Sponsors

Klinik für Anästhesiologie und Operative Intensivmedizin, Uniklinikum Köln
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: • Admission to an intensive care unit • Evidence of pleural effusion (unilateral / bilateral) • No contraindications for the usage of the EIT belt • Patients receive EIT monitoring to monitor their ventilation, monitor their weaning process or monitor non-invasive ventilation.

Exclusion criteria

Exclusion criteria: • No pleural effusion detectable • Immobilization (e.g. unstable spinal trauma / ribs / Sternal fractures, pelvic fractures, etc.) prohibit the use of a belt for the EIT measurement • Patients with a pacemaker, cardioverter (ICD) or other electrical pacemakers, which are powered by the alternating current of the EIT measurement could be impaired in its function. • Patients with skin lesions in the area of the EIT belt location.

Design outcomes

Primary

MeasureTime frame
- Quantification of pleural effusion with ultrasound or computed tomography - Quantification of pleural effusion after drainage (open surgical or via puncture)

Secondary

MeasureTime frame
- Detection of a “residual” pleural effusion despite drainage - Quantification of pleural effusion after drainage (osurgical drainage or drainage via puncture) via ultrasound

Countries

Germany

Contacts

Public ContactSandra Emily; Stoll;

Klinik für Anästhesiologie und Operative Intensivmedizin, Uniklinikum Köln;"Studiensponsor" Qualitaetssicherung fuer klinische Studien, Prodekanat Wissenschaft der Medizinischen Fakultaet, Zentrum fuer klinische Studien Koeln

sandra.stoll@uk-koeln.de;uni-sponsor@uk-koeln.de+491735697566;+49221478888154

Outcome results

None listed

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