Frequency and formation of central venous catheter induced thrombosis

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00020256

Enrollment

500

Registered

2019-12-19

Start date

2019-09-02

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

I80

Interventions

Group 1: Intensive care patients with the indication for central venous line (CVL) are examined before performing central venous Access and daily by ultrasound for a possible thrombus at the CVL or in

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. informed consent of patients aged 18 and older 2. Consent of the supervisors/precautionary agents

Exclusion criteria

Exclusion criteria: 1. Rejection by the patient/members/caregivers/precautionary agents 2. Emergency indication (e.g. cardiopulmonary resuscitation, acute danger to life)

Design outcomes

Primary

Measure	Time frame
1. Frequency and formation of central venous catheter induced thrombosis 2. Timing of thrombusformation in dependence of diagnoses/risk factors	—

Secondary

Measure	Time frame
1. Frequency of central venous thrombosis in dependence of catheter material 2. Frequency of wire malpositions during CVL-procedure	—

Countries

Germany

Contacts

Public ContactPeter Schwarzkopf

Sana Klinikum BornaKlinik für Anästhesie, Intensivmedizin, Schmerztherapie und Palliativmedizin

Peter.Schwarzkopf@sana.de03433212687

Outcome results

None listed

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