Registry for recording risk factors and complications in interventional ultrasound

Registry for recording risk factors and complications in interventional ultrasound - INVUS-registry

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00033134

Enrollment

Registered

2023-11-28

Start date

2024-12-02

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

Interventional ultrasound

Interventions

Group 1: Prospective registry to record intervention data in patients undergoing ultrasound-guided diagnostic or therapeutic procedures in the abdominal, thoracic or vascular region

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: - Continuous ultrasound guided intervention - Percutaneous and endosonographic interventions - Diagnostic interventions (e.g. fluid or tissue removal) - Therapeutic interventions (e.g. drainage, ablation, sclerotherapy, marking procedures, vascular access) - Outpatients and inpatients Intervention areas (modules): Thorax including mediastinum, abdomen including retroperitoneum and small pelvis, extra-abdominal interventions (e.g. lymph nodes), thyroid, nerve system, vascular system, musculoskeletal system (incl. joints, soft tissues, etc.), further modules are possible based on user requirements and initial evaluation data in the course of the procedure

Exclusion criteria

Exclusion criteria: - Diagnostic or therapeutic ascites and pleural punctures (incl. catheter insertion < 2 h) - Transrectal interventions of the prostate - Interventions of the breast - Prenatal interventions - Missing agreement for data collection

Design outcomes

Primary

Measure	Time frame
Recording of frequency and method spectrum of INVUS procedures, Process and outcome quality of the INVUS procedures, Frequency of immediate and delayed complications (including bleeding and infection events), predictors of adverse events and inadequate intervention results, efficiency of prevention methods for complications, criteria for the indication of various INVUS procedures, comparison of the effectiveness and risk of percutaneous (US) and endoscopic (EUS) guided interventions	—

Measure

Time frame

Recording of frequency and method spectrum of INVUS procedures, Process and outcome quality of the INVUS procedures, Frequency of immediate and delayed complications (including bleeding and infection events), predictors of adverse events and inadequate intervention results, efficiency of prevention methods for complications, criteria for the indication of various INVUS procedures, comparison of the effectiveness and risk of percutaneous (US) and endoscopic (EUS) guided interventions

—

Secondary

Measure	Time frame
Comparison of the quality of care in different facilities depending on the caseload, range of indications and investigator experience	—

Countries

Germany

Contacts

Public ContactDieter Nürnberg

Medizinische Hochschule Brandenburg Theodor Fontane Brandenburgisches Institut für Klinischen Ultraschall (BIKUS)

nuernbergdieter@gmx.de03391 141710

Outcome results

None listed

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