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

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

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12605000347662
Enrollment
300
Registered
2005-09-09
Start date
2004-12-06
Completion date
Unknown
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief 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.

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 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 D

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.

Sponsors

Mazda Foundation - Private Bag 40, Mount Waverley BC, Vic 3149
Lead SponsorCharities/Societies/Foundations

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

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.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026