Open-label nondeceptive placebo analgesia is blocked by the opioid antagonist naloxone.
Fabrizio BenedettiAziz ShaibaniClaudia ArduinoWilma ThoenPublished in: Pain (2022)
Open-label placebos, or placebos without deception, have been found to induce analgesia, a challenging concept that need to be investigated in detail. In particular, what we need to know is the mechanism through which analgesia is induced when no deception is involved. In this study, we show for the first time that open-label placebo analgesia can be reversed by the opioid antagonist naloxone, as already shown for deceptive placebos. To do this, we used the tourniquet technique to induce experimental ischemic arm pain. The open-label placebo challenge started when pain scores reached 7 on a 0 to 10 rating scale. Although 59.4% of the subjects did not respond to the open-label placebo, 40.6% showed a substantial response. On the basis of the natural history control group, a placebo responder reported pain scores equal to or less than 7 after 9 minutes from the open-label placebo administration. In these responders, we found that a hidden injection of 10 mg naloxone could reverse placebo analgesia compared with a hidden injection of saline solution. At least 2 control groups showed that naloxone per se was not hyperalgesic, thus ruling out naloxone-induced hyperalgesia as a confounding variable. In light of the need to better understand open-label placebo effects, these findings represent the first experimental evidence that nondeceptive placebo analgesia may be mediated by the same mechanisms as deceptive placebo analgesia, namely the endogenous opioid systems.
Keyphrases
- open label
- phase iii
- pain management
- chronic pain
- phase ii
- clinical trial
- double blind
- ultrasound guided
- phase ii study
- postoperative pain
- study protocol
- placebo controlled
- neuropathic pain
- diabetic rats
- randomized controlled trial
- spinal cord
- squamous cell carcinoma
- radiation therapy
- spinal cord injury
- ischemia reperfusion injury