Opioid Induced Hyperalgesia (OIH) Modulation With Propranolol

Pontificia Universidad Catolica de Chile

Status and phase: Unknown; Phase 4

Conditions: Hyperalgesia

Treatments: Drug: Propranolol; Drug: Saline

Study type: Interventional

Funder types: Other

Identifiers

NCT02934763

16-145

Details and patient eligibility

About

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.

Full 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.

Enrollment: 80 estimated patients

Sex: All

Ages: 18 to 65 years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

---

80 participants in 3 patient groups, including a placebo group

Placebo

Placebo Comparator group

Description:

Saline solution by target controlled infusion

Treatment:

Drug: Saline

Propranolol at 5ng/ml target dose

Active Comparator group

Description:

Propranolol iv by target controlled infusion, to achieve a plasmatic concentration of 5ng/ml

Treatment:

Drug: Propranolol

Propranolol at 15ng/ml target dose

Active Comparator group

Description:

Propranolol iv by target controlled infusion, to achieve a plasmatic concentration of 15ng/ml

Treatment:

Drug: Propranolol