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NCT05173090 Clinical Trial

Influence of Intra-abdominal Ropivacaine 0.5% Spray on Postoperative Analgesia in Laparoscopic Surgery.

Pain, Acute Clinical Trial

Official title:
Influence of Intra-abdominal Ropivacaine 0.5% Spray on Postoperative Analgesia in Laparoscopic Surgery.

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT05173090
Other study ID # Ropicoelio
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date January 15, 2022
Est. completion date July 30, 2022

Study information
Verified date November 2021
Source University of Liege
Contact Benjamin Javillier, MD
Phone +32498573882
Email javillier.benjamin@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Assessing postoperative pain after ropivacin 0.5% spray in the abdominal cavity during laparoscopic surgery.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 120
Est. completion date July 30, 2022
Est. primary completion date June 30, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Appendectomy or cholecystectomy surgery Exclusion Criteria: - Allergy to local anesthetics - Intolerance to tramadol HCl - Patient with peritonitis - Pregnant women - Surgery without laparoscopy - Chronic pain before the operation

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Ropivacaïne 0,5% for appendectomy or cholecystectomy surgery
Visual analog scale 15 min after arrival in the recovery room, then H+4, H+6, H+12, H+24 and one week after the operation

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
University of Liege

Outcome
Type Measure Description Time frame Safety issue
Primary Patient's pain The patient's satisfaction was assessed by visual analog scale, ranging from one (worse outcome )to four (better outcome During appendectomy and cholecystectomy surgery
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