Opioid Induced Hyperalgesia (OIH) Modulation With Propranolol
Primary Purpose
Hyperalgesia
Status
Unknown status
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Propranolol
Saline
Sponsored by
About this trial
This is an interventional treatment trial for Hyperalgesia
Eligibility Criteria
Inclusion Criteria:
- Patients scheduled for elective laparoscopic cholecystectomy
- American Society of Anesthesiology Score (ASA) I-II
Exclusion Criteria:
- Medical history of cardiac disease
- Medical history of respiratory disease
- Regular use of beta blockers
- Known allergies to drugs used in the study
- Known history of illicit drugs use
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Placebo Comparator
Active Comparator
Active Comparator
Arm Label
Placebo
Propranolol at 5ng/ml target dose
Propranolol at 15ng/ml target dose
Arm Description
Saline solution by target controlled infusion
Propranolol iv by target controlled infusion, to achieve a plasmatic concentration of 5ng/ml
Propranolol iv by target controlled infusion, to achieve a plasmatic concentration of 15ng/ml
Outcomes
Primary Outcome Measures
Postoperative opioid use
Dose of opioid required to manage pain adequately
Secondary Outcome Measures
Pain thresholds (heat)
Evaluation of the threshold to perceive a heat perception as pain
Pain thresholds (cold)
Evaluation of the threshold to perceive a cold perception as pain
Pain thresholds (tactile sensitivity)
Evaluation of pain by tactile sensitivity, using the PinPrick system
Temporal changes in pain sensibility
Evaluation of pain by tactile sensitivity, using the PinPrick system
Full Information
NCT ID
NCT02934763
First Posted
September 12, 2016
Last Updated
October 26, 2016
Sponsor
Pontificia Universidad Catolica de Chile
1. Study Identification
Unique Protocol Identification Number
NCT02934763
Brief Title
Opioid Induced Hyperalgesia (OIH) Modulation With Propranolol
Official Title
Opioid Induced Hyperalgesia (OIH) Modulation With Propranolol, in Laparoscopic Abdominal Surgery
Study Type
Interventional
2. Study Status
Record Verification Date
October 2016
Overall Recruitment Status
Unknown status
Study Start Date
October 2016 (undefined)
Primary Completion Date
April 2017 (Anticipated)
Study Completion Date
May 2017 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Pontificia Universidad Catolica de Chile
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Opioid Induced Hyperalgesia (OIH) is an entity than has been demonstrated in healthy volunteers and in animal models. Is defined as an increase in the perception to painful stimuli, increasing the opioid requirements and diminishing the pain thresholds to stimuli.
The apparition of OIH is also related to the exposure to opioids during surgery, depending of the dose, the time of exposition and the type of opioid.
This condition can be modulated, specially in the perioperative context. It has been seen in healthy volunteers and in animal models, than the use of propranolol can modulate this phenomena, diminishing the postoperative requirements of analgesia. It is also unknown, the dose of propranolol required to modulate adequately OIH.
The objective of this work is to evaluate the efficacy of propranolol in the modulation of opioid induced hyperalgesia, with lower postoperative requirements of analgesia rescue.
Detailed Description
This is a randomized controlled study, comparing 2 interventions with a placebo. The interventions will be use of propranolol, at different doses, to achieve specific plasmatic concentrations.
80 patients will be required to find a difference of 20% in the primary outcome.
The primary outcome to be measured is the postoperative use of opioids in the post anesthesic care unit.
Secondary outcomes, will be the amount of opioids used in the following 24 hours to the surgery, the time to the first dose of analgesia in the post anesthesic care unit, and the change in the pain thresholds, evaluated as pain by pressure and by tactile sensitivity, before and after surgery.
Also, as a secondary outcome, in a group than will not receive the study drug, we will evaluate the temporal changes in opioid induced hyperalgesia, by pain sensitivity measured in the postoperative hours 2, 4 and 24. 10 patients receiving placebo will be part of this additional measures.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hyperalgesia
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
80 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Saline solution by target controlled infusion
Arm Title
Propranolol at 5ng/ml target dose
Arm Type
Active Comparator
Arm Description
Propranolol iv by target controlled infusion, to achieve a plasmatic concentration of 5ng/ml
Arm Title
Propranolol at 15ng/ml target dose
Arm Type
Active Comparator
Arm Description
Propranolol iv by target controlled infusion, to achieve a plasmatic concentration of 15ng/ml
Intervention Type
Drug
Intervention Name(s)
Propranolol
Other Intervention Name(s)
Beta blocker
Intervention Description
propranolol iv by target controlled infusion, to achieve specific plasmatic concentration goals
Intervention Type
Drug
Intervention Name(s)
Saline
Other Intervention Name(s)
Placebo
Intervention Description
Saline as placebo
Primary Outcome Measure Information:
Title
Postoperative opioid use
Description
Dose of opioid required to manage pain adequately
Time Frame
24 hours posterior to surgery
Secondary Outcome Measure Information:
Title
Pain thresholds (heat)
Description
Evaluation of the threshold to perceive a heat perception as pain
Time Frame
24 hours posterior to surgery
Title
Pain thresholds (cold)
Description
Evaluation of the threshold to perceive a cold perception as pain
Time Frame
24 hours posterior to surgery
Title
Pain thresholds (tactile sensitivity)
Description
Evaluation of pain by tactile sensitivity, using the PinPrick system
Time Frame
24 hours posterior to surgery
Title
Temporal changes in pain sensibility
Description
Evaluation of pain by tactile sensitivity, using the PinPrick system
Time Frame
24 hours posterior to surgery
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients scheduled for elective laparoscopic cholecystectomy
American Society of Anesthesiology Score (ASA) I-II
Exclusion Criteria:
Medical history of cardiac disease
Medical history of respiratory disease
Regular use of beta blockers
Known allergies to drugs used in the study
Known history of illicit drugs use
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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Opioid Induced Hyperalgesia (OIH) Modulation With Propranolol
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