RecruitingNot ApplicableNCT07717151

Prevention of Chronic Postsurgical Pain in Chronic Opioid Users:

Ransitional Teleconsultation to Prevent Chronic Postsurgical Pain in Chronic Opioid Users


Sponsor

Centre Hospitalier Universitaire, Amiens

Enrollment

354 participants

Start Date

Jan 14, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

Chronic opioid users undergoing surgery are at increased risk of CPSP, contributing to long-term disability, decreased quality of life, and prolonged opioid exposure. Existing preventive strategies remain limited, and early postoperative monitoring may represent a key opportunity for intervention. Evidence suggests that transitional pain services can improve outcomes by optimizing pain control and reducing long-term opioid consumption, but implementation is heterogeneous and often resource-intensive. Telemedicine offers a scalable alternative, enabling early specialized evaluation and timely therapeutic adjustments while maintaining accessibility. This randomized controlled trial will compare standard postoperative follow-up with standard follow-up plus a specialized teleconsultation performed between postoperative day 15 and 28. The intervention aims to detect insufficiently controlled pain, signs of neuropathic pain, or maladaptive opioid use, and to propose individualized therapeutic adjustments when required. Participants will be followed for 6 months. Primary assessment will occur at 3 months to determine CPSP incidence. Secondary assessments will include pain trajectory (intensity, neuropathic features, functional interference), opioid consumption and misuse, quality of life, and a descriptive medico- economic evaluation


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying specialized teleconsultation and standard institutional perioperative management for people with chronic opioid users, chronic postsurgical pain, and other related conditions. The study is currently recruiting participants at 1 location.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHERstandard institutional perioperative management

standard institutional perioperative management

OTHERspecialized teleconsultation

Patients in the intervention arm participate in a specialized teleconsultation between postoperative day 15-28 to detect poorly controlled pain, neuropathic features, or opioid-related concerns, and to adjust treatment if needed.


Locations(1)

CHU Amiens-Picardie

Amiens, France

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NCT07717151


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