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Efficacy of Multimodal Opioid Therapy During Hepatic Resection Surgery (RITM-IVM)

Primary Purpose

Liver Dysfunction, Pain

Status
Unknown status
Phase
Not Applicable
Locations
Ireland
Study Type
Interventional
Intervention
Morphine sulphate
Morphine hydrochloride, remifentanil hydrochloride
Sponsored by
St Vincent's University Hospital, Ireland
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Liver Dysfunction focused on measuring Intrathecal morphine ITM intravenous morphine remifentanil hepatic resection, Adult, ASA I-III (stable), Liver dysfunction requiring primary parenchymal resection

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Adult
  • ASA I, II or stable III
  • Undergoing primary elective hepatic resection of < 50% predicted parenchymal resection

Exclusion Criteria:

  • Previous major upper GI surgery:

    • liver resection or transplant
    • gastrectomy
    • oesophagectomy
    • Whipple's procedure
  • Contraindications to dural puncture:

    • coagulopathy
    • uncorrected anti-coagulant therapy
    • spinal deformity
    • neurological disorder
    • psychiatric disorder
  • Morphine allergy
  • Co-morbidity predisposing to failure of extubation at conclusion of surgery:

    • severe cardiopulmonary pathology scoring ASA III (unstable)
    • IV
    • V
    • sleep apnoea
    • morbid obesity (BMI > 35)
  • Failure to proceed with resection, emergency resection or conversion to > 50% parenchymal resection
  • Chronic/intractable pain conditions:

    • requiring long-term high dose analgesia
    • implanted analgesic devices
  • Predisposition to severe post-operative nausea and vomiting:

    • motion sickness
    • previous PONV
  • Anatomical or physiological indication for rapid sequence induction (relative)

Sites / Locations

  • St. Vincent's University HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

1

2

Arm Description

IV morphine group

Remifentanil-intrathecal morphine group

Outcomes

Primary Outcome Measures

Opioid-related side effects

Secondary Outcome Measures

IV opioid analgesic supplementation

Full Information

First Posted
November 2, 2007
Last Updated
December 30, 2008
Sponsor
St Vincent's University Hospital, Ireland
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1. Study Identification

Unique Protocol Identification Number
NCT00553553
Brief Title
Efficacy of Multimodal Opioid Therapy During Hepatic Resection Surgery
Acronym
RITM-IVM
Official Title
Efficacy Of IV Morphine vs Remifentanil-Intrathecal Morphine Analgesia During Hepatic Resection Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
December 2008
Overall Recruitment Status
Unknown status
Study Start Date
September 2007 (undefined)
Primary Completion Date
May 2008 (Anticipated)
Study Completion Date
June 2008 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
St Vincent's University Hospital, Ireland

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The patient population requiring hepatic resection can demonstrate an unpredictable risk of exhibiting peri-operative coagulopathy resulting either from the pre-operative hepatic pathophysiology or volume of parenchymal resection. Choice of analgesia can be severely limited. Currently, the most commonly described use of combined remifentanil infusion and intrathecal morphine has been in fast-track cardiac surgery. To date, there are no published data describing its use in the context of major hepatobiliary where the investigators predict it may provide adequate analgesia with a lower rate of adverse effects over the first 24 hours after surgery.
Detailed Description
Choice of analgesia in hepatic resection surgery can be severely limited. This can depend upon on the pre-operative hepatic pathophysiology or the extent of parenchymal resection, both of which will affect peri-operative hepatic function, capacity for drug handling and risk of coagulopathy. Use of IV morphine during hepatic resection can result in high plasma levels post-operatively due to a reduced rate of morphine metabolism, risking a higher rate of morbidity. However, this remains a mainstay of peri-operative analgesia in combination with controversial non-opioid supplementation (paracetamol, non-steroidal anti-inflammatory drugs). This study compares the efficacy of IV morphine only versus a combination of pre-incisional intrathecal morphine and intra-operative IV remifentanil. Intrathecal morphine provides the mainstay of post-operative analgesia for 12-24 hours and remifentanil provides profound, titratable intra-operative analgesia until the delayed onset of the intrathecal morphine. We hypothesise that this combination might provide desirable intra-operative haemodynamic conditions and eliminate the post-operative additive effects of long-acting, intra-operative IV opioid and intrathecal morphine. Further, if the dose of intrathecal morphine is adequate, this would result in a low rate of post-operative analgesic supplementation and fewer side effects. The titratable dose range of remifentanil is limited to the lower range found to risk post-operative hyperalgesia.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Liver Dysfunction, Pain
Keywords
Intrathecal morphine ITM intravenous morphine remifentanil hepatic resection, Adult, ASA I-III (stable), Liver dysfunction requiring primary parenchymal resection

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
45 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
IV morphine group
Arm Title
2
Arm Type
Experimental
Arm Description
Remifentanil-intrathecal morphine group
Intervention Type
Drug
Intervention Name(s)
Morphine sulphate
Intervention Description
Intravenous morphine titrated up to 0.25 milligrams/kilogram prior to end of resection phase or within first 2 hours of surgery
Intervention Type
Drug
Intervention Name(s)
Morphine hydrochloride, remifentanil hydrochloride
Intervention Description
Pre-induction intrathecal morphine HCl (< 3 attempts), single shot via 25 G pencil point spinal needle at 10 micrograms/kilogram Intra-operative intravenous remifentanil HCl at titratable dose range 0.1-0.25 micrograms/kilogram/minute until start of wound closure
Primary Outcome Measure Information:
Title
Opioid-related side effects
Time Frame
First 24 hours post-operatively
Secondary Outcome Measure Information:
Title
IV opioid analgesic supplementation
Time Frame
First 24 hours post-operatively

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult ASA I, II or stable III Undergoing primary elective hepatic resection of < 50% predicted parenchymal resection Exclusion Criteria: Previous major upper GI surgery: liver resection or transplant gastrectomy oesophagectomy Whipple's procedure Contraindications to dural puncture: coagulopathy uncorrected anti-coagulant therapy spinal deformity neurological disorder psychiatric disorder Morphine allergy Co-morbidity predisposing to failure of extubation at conclusion of surgery: severe cardiopulmonary pathology scoring ASA III (unstable) IV V sleep apnoea morbid obesity (BMI > 35) Failure to proceed with resection, emergency resection or conversion to > 50% parenchymal resection Chronic/intractable pain conditions: requiring long-term high dose analgesia implanted analgesic devices Predisposition to severe post-operative nausea and vomiting: motion sickness previous PONV Anatomical or physiological indication for rapid sequence induction (relative)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Debbie A. D'Oyley, MB BS
Phone
+3531 2094262
Email
doyleyda@aol.com
First Name & Middle Initial & Last Name or Official Title & Degree
Neil J. McDonald, MB BCh
Phone
+3531 2094262
Email
n.mcdonald@svuh.ie
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Neil J. McDonald, MB BCh
Organizational Affiliation
St Vincent's University Hospital, Ireland
Official's Role
Principal Investigator
Facility Information:
Facility Name
St. Vincent's University Hospital
City
Dublin
State/Province
County Dublin
ZIP/Postal Code
4
Country
Ireland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Neil J. McDonald, MB BCh

12. IPD Sharing Statement

Learn more about this trial

Efficacy of Multimodal Opioid Therapy During Hepatic Resection Surgery

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