Status:
COMPLETED
Comparison of Administation Routes of Ropivacaine
Lead Sponsor:
Universiteit Antwerpen
Conditions:
Postoperative Pain
Eligibility:
FEMALE
18-70 years
Phase:
PHASE4
Brief Summary
The purpose of this study is to evaluate the effect of different routes of local anaesthesia administration in laparoscopic procedures to reduce post-operative pain (intra-peritoneal infusion of Ropiv...
Detailed Description
Research Question What is the best route of Ropivacaine administration in laparoscopic procedures in decreasing post-operative pain? Is it port site injection, intra-peritoneal instillation of local a...
Eligibility Criteria
Inclusion
- Elective gynecologic laparoscopy for benign conditions at Antwerp University Hospital.
- Successful laparoscopy without surgical or anesthetic complications.
- Female
- 18-70 years
- ASA I-II
Exclusion
- Hypersensitivity to anaesthetics of the amide-type
- Obesity, BMI \> 35
- Patients with chronic use of analgesics / chronic pain
- Patients with an abnormal liver function
- Urgent surgical procedures
- Pregnancy (this means we only include patients who use contraceptives, are sterilized, have a negative dipstick testing or a negative serum testing or patients who are postmenopausal)
Key Trial Info
Start Date :
July 1 2017
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
February 29 2020
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT04459026
Start Date
July 1 2017
End Date
February 29 2020
Last Update
July 7 2020
Active Locations (1)
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1
UZA
Edegem, Antwerp, Belgium, 2650