None listed
Conditions
Brief summary
This is a pilot study looking into safety of giving bolus of ropivacaine followed by continous infusion for 48 hrs in Transversus Abdominis Plane Block. Safety of this regime will be established by serial blood samples to analyse toal & free ropivacaine concentration , Serail ECG 's looking into QTc interval & patient will be observed for sign & symptoms of Local anaesthetic toxicity
Interventions
Sponsors
Study design
Eligibility
Inclusion criteria
Elective/Emergency abdominal surgery Between 18 and 80 years of age ASA less than 4 Adequate English language skills
Exclusion criteria
1 Allergy to local anaesthetic 2 Pt refusal 3 ASA score > 4 (i.e 4,5) 4 Pregnancy 5 On regular opioid medication or any other medication for chronic pain management. 6 Mental handicap or psychiatric condition precluding adequat communication. 7 Patients taking ciprofloxacin & fluvoxamine (affects the metabolism of LA) 8 Qt c interval > 0.45 sec in males and > 0.47 sec in females 9 Drugs affecting Qtc interval e.g. Haloperidol, Amiodarone, Sotaol