Visualization of the catheter orifice position for Patient Controlled Analgesia using Carbon dioxide contrast-enhanced ultrasonography, to check the spread of the chemical research

JRCT ID: jRCT1090220253

Registered date:20/06/2016

Basic Information

• Recruitment status: COMPLETED

Health condition(s) or Problem(s) studied

Rotator Cuff Tear
Impingement syndrome
Frozen shoulder
Osteoarthritis of the shoulder
Reccurent Dislocated shoulder
fracture of shoulder

• Date of first enrollment: 02/03/2016
• Target sample size: 30
• Countries of recruitment: Japan
• Study type: Interventional

Intervention(s)

Intervention type:DEVICE,PROCEDURE
Name of intervention:Single arm
Dose form / Japanese Medical Device Nomenclature:DEVICE
Route of administration / Site of application:PERINEURAL
Dose per administration:4ml
4ml/h
4ml/h
Dosing frequency / Frequency of use:PRN
For Tuen
Planned duration of intervention:24hour
Intended dose regimen:A ropivacaine 0.25% 4 ml/hour infusion with mandatory 24 hours
detailes of teratment arms:
Comparative intervention name:
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Outcome(s)

• Primary Outcome: VAS,sensory,MMT

Key inclusion & exclusion criteria

• Age minimum: Not applicable
• Age maximum: Not applicable
• Gender: Both
• Include criteria: Patients undergoing a shoulder joint surgery, obtained the consent
• Exclude criteria: Patients with oral anti-platelet drugs

Related Information

• Primary Sponsor: SHIMIZU HAYATO
• Source(s) of Monetary Support: Self-procurement
• Secondary ID(s): UMIN000022702,JMA-IIA00253