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Dependence of Splanchnic Perfusion on PEEP and Intraabdominal Pressure

Dependence of Splanchnic Perfusion on PEEP and Intraabdominal Pressure - DoSPo-PIP

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00023895
Enrollment
20
Registered
2021-02-15
Start date
2021-02-19
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

D32.9

Interventions

Group 1: During the postperative phase of an elective operation, a PEEP trial is carried out after consent has been given to the study. Blood gas analysis, intra-abdominal pressure measurement, and ul

Sponsors

Universitätsmedizin Göttingen Klinik für Anästhesiologie
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: • Female, male and diverse patients • Age> 18 years 75ml / min)

Exclusion criteria

Exclusion criteria: • Age 80 years • Lack of consent • Increased intra-abdominal pressure at baseline • Impairment of pulmonary function / need for a high PEEP at baseline • Severe arterio-occlusive disease • Renal artery stenosis • history of Nephrectomy / Splenectomy • Renal insufficiency (eGFR 30) • history of abdominal surgery

Design outcomes

Primary

MeasureTime frame
Differences in renal and splanchnic resistance index

Countries

Germany

Contacts

Public ContactLars-Olav Harnisch

Universitätsmedizin Göttingen Klinik für Anästhesiologie

lars-olav.harnisch@med.uni-goettingen.de05513963579

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: May 21, 2026