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Liver function, quantified by LiMAx test, after major abdominal and thoracic surgery. Comparison between open and laparoscopic approach.

Liver function, quantified by LiMAx test, after major abdominal and thoracic surgery. Comparison between open and laparoscopic approach. - LiSon Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00012247
Enrollment
25
Registered
2021-01-11
Start date
2014-03-25
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

esophageal resection, gastric resection

Interventions

Group 1: Surveillance of live function by LiMaX test in patients with open and laparoscopic throraco-abdominal surgery. Comparison with the ICG test and static live Parameter. Korrelation with live pe

Sponsors

Charité Campus Virchow-Klinikum
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: transhiatal extended gastrectomy or esophagectomy.

Exclusion criteria

Exclusion criteria: pre-existing liver diseases (e. g. cirrhosis Child-Pough II-III), severe complications within the first ten days after surgery (Dindo IV°), allergy against substances used in the test, missing informed consent

Design outcomes

Primary

MeasureTime frame
Liver function measured by LiMAx test, preoperative between day 1-3 before scheduled operation and postoperative days 1, 3, 5 and 10.

Secondary

MeasureTime frame
Comparison with Indocyaningreen-test (Indocyaningreen-plasma-dilution-rate) 1-3 days preoerative and postoperative at day 1, 3, 5 and 10 and Duplex sonography (peak velocity of the Arteria hepatica and flow volume of the Vena Portae) 1-3 days preoperatve and postoperative on day 1, 3, 5 and 10.

Countries

Germany

Contacts

Public ContactMagnus Kaffarnik

Charite - Universitätsmedizin Berlin, Campus Virchow Klinik für Allgemein, Viszeral- und Transplantationschirurgie

magnus.kaffarnik@charite.de+40(0)30450652235

Outcome results

None listed

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