NIPH Clinical Trials Search

JAPANESE
国立保健医療科学院
UMIN ID: UMIN000048057

Registered date:01/07/2022

The effectiveness of anesthesia for percutaneous transluminal angioplasty in arteriovenous fistula on the reduction of pain

Basic Information

Recruitment status Recruiting
Health condition(s) or Problem(s) studiedPain during percutaneous transluminal angioplasty
Date of first enrollment2022/07/01
Target sample size40
Countries of recruitmentJapan
Study typeInterventional
Intervention(s)blind technique under ultrasound guidance

Outcome(s)

Primary OutcomePain visual analog scale score of the pain
Secondary Outcomeheart rate, time required for the anethesia, side effect of the anesthesia

Key inclusion & exclusion criteria

Age minimum20years-old
Age maximumNot applicable
GenderMale and Female
Include criteria
Exclude criteria1)Patients who have never undergone PTA 2)Patients who did not undergo PTA more than twice during the study period 3)Patients who were unable to assess the pain (communication disability, psychiatric disorder, dementia, and sensory impairment)

Related Information

Contact

public contact
Name Akihiro Kosoku
Address Miyakenishi 1-358-3, Matsubara-shi, Osaka, Japan Japan 580-0045
Telephone 072-334-8558
E-mail aki.kosoku@gmail.com
Affiliation Meijibashi hospital Department of urology
scientific contact
Name Akihiro Kosoku
Address Miyakenishi 1-358-3, Matsubara-shi, Osaka, Japan Japan
Telephone 072-334-8558
E-mail aki.kosoku@gmail.com
Affiliation Meijibashi hospital Department of urology