Hepatic Excision and Ablation Log

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity Hospital, Antwerp

About this trial

This study aims to establish a registry for liver surgery and ablation procedures to improve patient care, advance research, and enhance surgical quality. The registry will collect pseudonymized data on patient demographics, disease characteristics, procedural details, and outcomes.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Both benign and malignant liver lesions are included

Disqualifiers

None

Trial population

All patients who will undergo liver surgery or ablation.

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

  • Liver surgery / ablation

    Procedure/Surgery

    Any type of liversurgery or CT-guidede liver ablation

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Establishment of a Liver Surgery and Ablation Registry

The primary objective of this study is to create a comprehensive registry of patients who have undergone liver surgery or liver ablation. This registry will serve as a foundation for future epidemiological studies, enabling the assessment of long-term outcomes, the identification of risk factors, and the evaluation of potential therapeutic interventions. Data collected will include demographic information, medical history, surgical details, postoperative outcomes, and survival rates. By compiling this data, we aim to better understand the patient population and improve care for individuals undergoing liver surgery or ablation.

Time frame
10 years

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: