NIPH Clinical Trials Search

JAPANESE
国立保健医療科学院
JMACCT ID: JMA-IIA00253

Registered date:20/06/2016

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

Basic Information

Recruitment status Completed
Health condition(s) or Problem(s) studiedRotator Cuff Tear Impingement syndrome Frozen shoulder Osteoarthritis of the shoulder Reccurent Dislocated shoulder fracture of shoulder
Date of first enrollment02/03/2016
Target sample size30
Countries of recruitmentJapan
Study typeINTERVENTIONAL
Intervention(s)Intervention type:DEVICE. Intervention1:Single arm, Dose form:DEVICE, Route of administration:PERINEURAL, intended dose regimen:A ropivacaine 0.25% 4 ml/hour infusion with mandatory 24 hours.

Outcome(s)

Primary OutcomeVAS,sensory,MMT. Timepoint:postoperative 24 hour.
Secondary Outcome.

Key inclusion & exclusion criteria

Age minimumNo Limit
Age maximumNo Limit
GenderBOTH
Include criteriaPatients undergoing a shoulder joint surgery, obtained the consent
Exclude criteriaPatients with oral anti-platelet drugs

Related Information

Contact

public contact
Name SHIMIZU HAYATO
Address orsopedics,osaka city hirano ku nagayoshinagahara 1-2-34
Telephone +81-6-6709-0301
E-mail hyt_1jd@yahoo.co.jp
Affiliation Nagayoshi General Hospital
scientific contact
Name SHIMIZU HAYATO
Address orsopedics,osaka city hirano ku nagayoshinagahara 1-2-34
Telephone +81-6-6709-0301
E-mail
Affiliation Nagayoshi General Hospital