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Postoperative Pain Control Using ON-Q Painbuster Pump

NCT01184794 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2013-11-13

No results posted yet for this study

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 levobupivacaine and efficacy will be measured using ranked ordinal pain scales and rescue oral analgesia use.

Conditions

  • Post Operative Analgesia

Interventions

DRUG

levobupivacaine

40 ml over 48 hours

Sponsors & Collaborators

  • Ashford and St. Peter's Hospitals NHS Trust

    lead OTHER

Principal Investigators

  • Jeremy T Wright, MD · Ashford and St. Peter's Hospitals NHS Trust

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
SINGLE_GROUP

Eligibility

Min Age
16 Years
Max Age
75 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-08-31
Primary Completion
2011-12-31
Completion
2011-12-31

Countries

  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01184794 on ClinicalTrials.gov