Status:
COMPLETED
Postoperative Pain Control Using ON-Q Painbuster Pump
Lead Sponsor:
Ashford and St. Peter's Hospitals NHS Trust
Conditions:
Post Operative Analgesia
Eligibility:
FEMALE
16-75 years
Phase:
PHASE3
Brief Summary
This study is a blinded randomised study of slow release levobupivacaine vs saline for women undergoing day case operative pelvic laparoscopy. Participants will be randomly given either saline or levo...
Detailed Description
METHOD: This is a triple-blinded randomised control study to determine whether a continuous intraperitoneal infusion of levobupivacaine 0.5%, when compared with normal saline 0.9%, in women undergoin...
Eligibility Criteria
Inclusion
- Women undergoing 'Day case' operative laparoscopic procedures.
- These women are deemed suitable to return home on the day of surgery, both in terms of physical fitness and their home circumstances.
Exclusion
- Women having laparoscopic procedures for diagnostic purposes or minor operations such as sterilisation, will be excluded from the study.
- These procedures are less likely to cause significant pain due to operation.
Key Trial Info
Start Date :
August 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2011
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT01184794
Start Date
August 1 2009
End Date
December 1 2011
Last Update
November 13 2013
Active Locations (1)
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1
Ashford & St Peter's Hospitals NHS Trust
Chertsey, Surrey, United Kingdom, KT16 0PZ