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NCT02827097 Clinical Trial

The Effect of Rectus Sheath Block on the Postoperative Analgesia in the Patients Undergoing Robotic Single Port Cholecystectomy

Gallbladder Diseases Clinical Trial

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT02827097
Other study ID # AJIRB-MED-CT4-16-127
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date October 2016
Est. completion date October 2016

Study information
Verified date July 2019
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 rectus sheath block on abdominal pain score after robotic single port cholecystectomy.

The secondary purpose of this study is to investigate the effect of rectus sheath block on fentanyl consumption during stay of recovery room after surgery.

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date October 2016
Est. primary completion date October 2016
Accepts healthy volunteers No
Gender All
Age group 20 Years to 80 Years
Eligibility Inclusion Criteria:

- robotic single Port cholecystectomy for gallbladder disease

Exclusion Criteria:

- Allergy to ropivacaine, infection, history of abdominal surgery, body mass index more than 30

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• denogan and rectus sheath block
administration of denogan and rectus sheath block with 0.375% ropivacaine
• denogan
administration of denogan

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 Abdominal pain score after surgery Change from baseline abdominal pain score up to 24 hours
Secondary Fentanyl consumption in recovery room Up to 1 hours
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