Recruiting NCT06766656

Comparison of Transverse and Longitudinal Incisions for Venous Access Port Placement

Trial Parameters

Condition Central Venous Access Devices

Sponsor Jagiellonian University

Study Type INTERVENTIONAL

Phase N/A

Enrollment 200

Sex ALL

Min Age 18 Years

Max Age 85 Years

Start Date 2025-02-01

Completion 2025-12-31

All Conditions

Central Venous Access Devices Implantable Venous Access Port

Interventions

Incision

Brief Summary

The aim of the study is to assess whether the direction of skin incision affects pain within the first 24 hours, patient comfort 7 days after the procedure, procedure time, and the occurrence of early complications related to vascular port implantation.

Eligibility Criteria

Inclusion Criteria: * Inclusion Criteria: Age \> 18 and \< 80 years Informed consent Need for central venous access port implementation under local anesthesia Exclusion Criteria: Impaired blood clotting Ongoing antiplatelet drugs therapy, except acetylsalicylic acid Trauma or surgical past history on both shoulder girdles Known central venous thrombosis (subclavian vein, upper vena cava) Known pneumothorax Chronic opioid use Septic state Agranulocytosis

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NCT06766656

Comparison of Transverse and Longitudinal Incisions for Venous Access Port Placement

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VIEW ON CLINICALTRIALS.GOV ↗ MORE CENTRAL VENOUS ACCESS DEVICES TRIALS