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NCT02827136 Clinical Trial

Effect of Lidocaine Patch for Shoulder Pain in Laparoscopic Cholecystectomy

Gallbladder Diseases Clinical Trial

Official title:
Ajou University School of Medicine

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02827136
Other study ID # AJIRB-MED-OBS-16-076
Secondary ID
Status Completed
Phase N/A
First received July 4, 2016
Last updated December 18, 2017
Start date February 8, 2017
Est. completion date September 27, 2017

Study information
Verified date December 2017
Source Ajou University School of Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The primary purpose of this study is to investigate the effect of lidocaine patch on the shoulder pain score after end of surgery.

The secondary purpose of this study is to investigate the effect of lidocaine patch on the total number of analgesic request on ward.

Recruitment information / eligibility
Status Completed
Enrollment 63
Est. completion date September 27, 2017
Est. primary completion date September 27, 2017
Accepts healthy volunteers No
Gender All
Age group 20 Years to 85 Years
Eligibility Inclusion Criteria:

- Laparoscopic cholecystectomy under general anesthesia

Exclusion Criteria:

- Infection, trauma, or bleeding on shoulder

- Allergy to lidocaine

- Chronic pain

- Renal dysfunction

- Liver dysfunction

- Seizure

- History of shoulder surgery

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Lidocaine patch and hypafix
Appliance of Lidocaine patch and hypafix on both shoulder tip after anesthetic induction
• hypafix
Appliance of hypafix on both shoulder tip after anesthetic induction

Locations
Country Name City State
Korea, Republic of Department of Anesthesiology and Pain Medicine, Ajou University School of Medicine Suwon Seoum

Sponsors (1)
Lead Sponsor Collaborator
Ajou University School of Medicine

Country where clinical trial is conducted

Korea, Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Primary Shoulder pain score Change from baseline shoulder pain score up to 24 hr after end of surgery
Secondary Total number of analgesics request on ward Up to postoperative day 3
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