ocal Anaesthetic Infusion for Laparoscopic Hysterectomy: A Randomised controlled trial
- Conditions
- women having a total laparoscopic or vaginally assisted laparoscopic hysterectomy
- Registration Number
- EUCTR2010-023754-37-GB
- Lead Sponsor
- Ashford and St Peters Hospitals NHS Trust
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Authorised-recruitment may be ongoing or finished
- Sex
- Female
- Target Recruitment
- Not specified
Inclusion Criteria
women undergoing total laparoscopic or laparoscopic assissted vaginal hysterectomy
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range
Exclusion Criteria
Women with a history of hypersensitivity to local anaesthetics.
Women undergoing hysterectomy for cancer.
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Main Objective: Need for 'rescue' analgesia in women who have an infusion of chirocaine compared to normal saline.;Secondary Objective: •Pain intensity (on movement and rest)<br>•Side effects from rescue analgesia<br>•Amount of patient controlled analgesia needed<br>•Hospital length of stay<br>•Patient satisfaction with pain relief<br>in women who have an infusion of chirocaine compared to normal saline.;Primary end point(s): Need for 'rescue' analgesia in women who have an infusion of chircocaine 0.5% compares to normal saline 0.9%
- Secondary Outcome Measures
Name Time Method