Prevention of Chronic Postsurgical Pain in Chronic Opioid Users:

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorCentre Hospitalier Universitaire, Amiens

About this trial

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 criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥18 years

Elective non-urgent surgery with expected moderate or higher postoperative pain

Chronic preoperative opioid use

Written informed consent

Disqualifiers

Ambulatory surgery

Endoscopic or palliative surgery

Patients receiving opioid substitution therapy

Non-medical opioid use

Trial design

Design model

Parallel

Treatments tested in this trial

  • standard institutional perioperative management

    Other intervention

    standard institutional perioperative management

  • specialized teleconsultation

    Other intervention

    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.

Treatment groups

354 Participants
are divided into 2 treatment groups
Group A: Standard care + specialized postoperative teleconsultationExperimental treatment 2 interventions
Group B: Standard postoperative care aloneActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Incidence of chronic postsurgical pain (CPSP)

Incidence of chronic postsurgical pain (CPSP) at 3 months, defined as: * new or aggravated postsurgical pain located at the surgical site or innervated territory, * persistent for ≥3 months, * intensity ≥3/10 (new pain) or increase ≥2/10 from baseline (aggravation), * with significant functional impact (≥3/10 on at least one Brief Pain Inventory interference item), * assessed at day 90 ±14.

Time frame
at 3 months

Secondary outcomes

1

Pain trajectory

Pain trajectory is measured by using intensity (BPI), + neuropathic features (DN4) +Quality of life (EQ-5D-5L)

Time frame
at 3 months
2

Pain trajectory

Pain trajectory is measured with intensity (BPI), neuropathic features (DN4), Quality of life (EQ-5D- 5L)

Time frame
at 6 months
3

Opioid use

Opioid use is defined as oral morphine equivalent consumption, proportion with reduction/discontinuation, POMI-5F, SOWS, DSM-5 OUD criteria

Time frame
at 3 months
4

Opioid use

Opioid use is defined as oral morphine equivalent consumption, proportion with reduction/discontinuation, POMI-5F, SOWS, DSM-5 OUD criteria

Time frame
at 6 months

Other outcomes

Sponsors and contacts

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