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NCT05189392: PICO-PTA

Efficacy of PICO Compared to Opsite Post-Op Visible on Surgical Wound in Patients at High Risk of Local Complications, Undergoing Hip Arthroplasty

Status unknown NA Last updated 12 January 2022
What this trial tests

NA trial testing PICO in Evaluate Postsurgical Hematoma in 42 participants. Status unknown.

Timeline
10 January 2022
Primary endpoint
10 December 2024
10 January 2025

Quick facts

Lead sponsorI.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment42
Start date10 January 2022
Primary completion10 December 2024
Estimated completion10 January 2025
Sites1 location across Italy

Drugs / interventions tested

Conditions studied

Sponsor

I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio — full company profile →

Who can join

Adults 55 to 85, any sex, with Evaluate Postsurgical Hematoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Evaluate the effect of the PICO medical device, compared to the Opsite Post-Op Visible medical device, in reducing the formation of postsurgical hematoma in the surgical wound of patients at high risk of local complications, undergoing hip arthroplasty

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of PICO

Trials testing the same drug.

Other I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05189392.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing