A Study to Analyze the Effects of Buprenorphine on Hyperalgesia in Patients with Opioid Use Disorder

Overview

Información sobre este estudio

The purpose of this study is to investigate the effects of buprenorphine on hyperalgesia (HP) perception in adults undergoing treatment for opioid use disorder (OUD).

Elegibilidad para la participación

Los requisitos de elegibilidad de los participantes incluyen la edad, el sexo, el tipo y el estadio de la enfermedad, y los problemas de salud o tratamientos previos. Las pautas difieren de un estudio a otro e identifican quiénes pueden o no pueden participar. No hay garantía de que cada persona elegible que desee participar en un ensayo se inscribirá. Comunícate con el equipo del estudio para analizar la elegibilidad del estudio y la posible participación.

Inclusion Criteria:

  • Age 18 to 70 years old.
  • Diagnosis of opioid use disorder.
  • Stable dose of buprenorphine or naltrexone for 7 days.
  • No pharmacotherapy for OUD for 7 days for individuals in the no pharmacotherapy group.

Exclusion Criteria

  • Medical or surgical conditions that could be adversely impacted by HP testing including, but not exclusively limited to, active psoriatic lesions at the site of testing, cellulitis at site of testing, and previous skin grafting at site of testing. Patients may be excluded for other comorbid medical or surgical conditions based on the physician investigator’s discretion.
  • History of schizophrenia, dementia, or other chronic psychiatric disorder that could be adversely impacted by study participation. Patients may be excluded for other comorbid mental health conditions based on the physician investigator’s discretion.
  • Inability to function independently in an ambulatory care setting due to severe deconditioning requiring use of supportive gait aids including a cane or walker.  Patients may be excluded for other functional problems based on the physician investigator’s discretion.
  • Signs and symptoms of opioid withdrawal syndrome.

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 5/14/2024. Questions regarding updates should be directed to the study team contact.

Sedes participantes de Mayo Clinic

Los estatus de los estudios cambian con frecuencia. Comunícate con el equipo del estudio para obtener la información más actualizada acerca de la posibilidad de participar.

Sede de Mayo Clinic Estatus Contacto

Rochester, Minn.

Investigador principal de Mayo Clinic

Tyler Oesterle, M.D., M.P.H.

Comunícate con nosotros para obtener el estatus más reciente

Contact information:

Danielle Zheng M.D., Ph.D.

(507)255-6219

Zheng.Danielle@mayo.edu

More information

Publicaciones

Publications are currently not available
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CLS-20467343

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