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Table 1 Inclusion and exclusion criteria

From: Effect of a high-dose target-controlled naloxone infusion on pain and hyperalgesia in patients following groin hernia repair: study protocol for a randomized controlled trial

Inclusion criteria

Exclusion criteria

• Healthy male (ASA I–II)

• Participant does not understand Danish

• 18 ≤ age ≤ 65 years

• Participant is not cooperative

• Patients submitted to elective, unilateral, primary, open groin herniarepair 6–8 weeks prior to study start

• Participant had previous surgery in the inguinal region

• Open surgical procedure by the Lichtenstein method

• Pain at rest > 3 (NRS, 0–10)

• Signed informed consent

• Activity-related pain in the surgical field > 5 (NRS, 0–10)

• 18 kg/m2 < BMI < 30 kg/m2

• Nerve lesions in the assessment sites (for instance, after trauma, disc herniation, etc.)

• Urine sample without traces of opioids (morphine, methadone, buprenorphine, codeine, tramadol, ketobemidone, oxycodone, hydromorphone, dextromethorphan)

• Skin or nerve lesions or tattoos in the assessment areas

 

• Regular use of analgesic drugs (≥ twice a week)

 

• Allergy against morphine or other opioids (including naloxone)

 

• Alcohol or drug abuse

 

• Use of psychotropic drugs (except SSRI)

 

• Neurological or psychiatric disease

 

• Chronic pain condition

 

• Use of prescription drugs 1 week before the experimental days

 

• Use of over-the-counter drugs 48 hours before the experimental days

  1. ASA American Society of Anesthesiology (physical status classification system), BMI body mass index, NRS numerical rating scale, SSRI selective serotonin reuptake inhibitors