Value of a preoperative volume/ function analysis for patient safety after extended partial liver resection

Value of a preoperative volume/ function analysis for patient safety after extended partial liver resection - FUSION

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00006160

Enrollment

Registered

2014-05-14

Start date

2008-10-18

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

C22.0 C22.1

Interventions

Group 1: 40 female or male patients (age greater 50) which are undergoing an oncologic partial liver resection an our department. In the frame of this study we measure preoperative liver function (sur

Eligibility

Sex/Gender

All

Age

50 Years to No maximum

Inclusion criteria

Inclusion criteria: - Patients suffering from maligne hepatobiliary disease - preoperative CT-imaging (examination date: max. 4 weeks prior inclusion) - informed consent

Exclusion criteria

Exclusion criteria: -Patients with previous liver surgery - Impaired renal function (elevated serum creatinine) - Contrast medium intolerance - Thyroid hypofunction (decreased TSH)

Design outcomes

Primary

Measure	Time frame
Evaluation of the reliability of preoperative evaluation of future remnant liver volume and future remnant liver function by comparison to really measured postoperative values.	—

Secondary

Measure	Time frame
Evaluation of perioperative factors associated with morbidity and mortality with respect to remnant volume and remnant liver function	—

Countries

Germany

Contacts

Public ContactMartin Stockmann

Charité - Universitätsmedizin Berlin

martin.stockmann@charite.de030 450 552 001

Outcome results

None listed

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