RecruitingPhase 3ACTRN12605000347662

Continuous infusion of local anaesthetic in the control of pain following colorectal surgery


Sponsor

Mazda Foundation - Private Bag 40, Mount Waverley BC, Vic 3149

Enrollment

300 participants

Start Date

Dec 6, 2004

Study Type

Interventional

Conditions

Summary

To determine if there is a better and safer option for pain relief following laparotomies for colorectal surgery, by using a continuous infusion of local anaesthetic into the wound.


Eligibility

Sex: Both males and femalesMin Age: 18 Yearss

Inclusion Criteria1

  • Undergoing open colorectal surgery (excluding abdomino-perineal resections) and that there is written informed consent.

Exclusion Criteria1

  • Allergies to lignocaine or ropivacaine, true allergy to morphine, epidural or intrathecal infusions, emergency surgery, and if the patient is mentally or legally incapacitated or if the have a prior history of altered mental state.

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Interventions

To determine whether continous local anaesthetic, ie. ropivacaine 1% (Naropin - produced by AstroZeneca) via a dual catheter PainBuster Soaker Pain Management System (produced by I-Flow) is a more eff

To determine whether continous local anaesthetic, ie. ropivacaine 1% (Naropin - produced by AstroZeneca) via a dual catheter PainBuster Soaker Pain Management System (produced by I-Flow) is a more effective form of post operative analgesia compared to traditional analgesias for midline incisions following major colorectal resections. The PainBuster Soaker System is tested in a randomised double blinded control study where participants either receive ropivacaine 1% or Saline in their PainBuster Device for the first three days. Both groups also receive a Morphine PCA, Tramadol, Ketorolac and Panadol.


Locations(1)

Australia

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ACTRN12605000347662