PUBLISHER: Mordor Intelligence | PRODUCT CODE: 1910449
PUBLISHER: Mordor Intelligence | PRODUCT CODE: 1910449
pain management market size in 2026 is estimated at USD 85.63 billion, growing from 2025 value of USD 81.92 billion with 2031 projections showing USD 106.86 billion, growing at 4.53% CAGR over 2026-2031.

Greater life expectancy, stringent opioid regulations and expanding use of connected neuromodulation platforms anchor this growth trajectory. Clinicians now favor multimodal regimens that blend non-opioid pharmacology with device-based therapies, a shift reinforced by payer incentives rewarding durable outcomes over pill counts. Digital health integration improves longitudinal monitoring, aligning treatment intensity with real-time patient-reported pain scores while curbing hospital readmissions. Heightened ESG scrutiny of legacy opioid makers meanwhile accelerates capital flows toward developers of non-addictive alternatives and AI-driven dosing algorithms.
Growing cohorts aged >= 45 now represent the highest incidence of chronic musculoskeletal and neuropathic complaints. In 2024, 24.3% of U.S. adults reported chronic pain, with prevalence peaking in the 65+ group. European meta-analysis places adult prevalence at 21.45%, propelled by diabetes, arthritis, and postsurgical syndromes. Patients living with persistent pain incur double the healthcare expenditure of age-matched peers and lose USD 12,167 annually in productivity within high-income countries. Payers, therefore, channel funds toward longitudinal programs combining pharmaceutical, device, and behavioral elements. Recognition of chronic pain as a standalone disease entity further unlocks dedicated reimbursement codes and specialty clinic capacity worldwide.
Landmark cost-utility studies show spinal cord stimulation paired with best medical therapy remains cost-effective over 10 years, outperforming pharmacologic management at typical willingness-to-pay thresholds. Dorsal root ganglion technology delivers even higher quality-adjusted life years for focal neuropathic syndromes, despite steeper upfront costs. Closed-loop platforms now auto-adjust amplitude based on evoked compound action potentials, sustaining analgesia as physiologic states shift. Regulatory bodies accelerate market entry through Breakthrough Device designations, trimming review times and incentivizing venture investment. Expanded reimbursement in select EU member states confirms recognition of durable neuromodulation value, increasing hospital purchasing confidence and physician adoption rates.
Implantable pulse generators priced between USD 20,000 - 50,000 per patient exceed many public-sector budgets in emerging economies. Replacement surgeries every 4-7 years add anesthesia and hospitalization charges, straining payer tolerance. Health technology assessment agencies now demand ten-year real-world evidence before approving high-cost neuromodulation reimbursement lines. Manufacturers react by migrating to rechargeable batteries and automated programming that lower clinician touchpoints. Leasing models and outcome-based contracts have begun surfacing, yet capital intensity remains a gating factor across low- and middle-income settings.
Other drivers and restraints analyzed in the detailed report include:
For complete list of drivers and restraints, kindly check the Table Of Contents.
Drugs retained 68.92% of pain management market share in 2025, anchored by NSAIDs, anticonvulsants and selective antidepressants used for neuropathic indications. Non-opioid innovations, including sodium-channel blockers, sustain momentum as guideline authors promote opioid-sparing regimens. In value terms, the drugs segment added USD 3.2 billion year-over-year, supported by strong generic uptake in Asia-Pacific and Latin America. Devices are set to outpace pharmaceuticals at a 9.99% CAGR, adding roughly USD 11 billion to the pain management market size by 2031.
Closed-loop spinal cord stimulators and dorsal root ganglion systems headline this surge, leveraging real-time physiologic feedback to fine-tune amplitude and pulse width. Analgesic infusion pumps shrink in form factor while gaining Bluetooth-enabled dosage logs that feed clinician dashboards. FDA Breakthrough Device designations granted in 2024 and 2025 shave six to nine months from review cycles, accelerating commercial rollout. As value-based procurement spreads, hospital buyers increasingly weigh total cost of ownership, a metric favoring rechargeable stimulators with extended battery life.
The Pain Management Market Report is Segmented by Mode of Pain Management (Drugs [Opioids and Non-Narcotic Analgesics] and Devices [Neuro-Modulation Devices and More]), Application (Neuropathic Pain, Cancer Pain, Facial Pain & Migraine and More), Setting of Care (Hospitals, Ambulatory Surgical Centers and More), and Geography (North America, Europe, Asia-Pacific, and More). The Market Forecasts are Provided in Terms of Value (USD).
North America retained 38.10% revenue in 2025, supported by mature reimbursement, extensive ASC networks and swift FDA clearance pathways. Continued litigation over opioid marketing drives diversification toward non-addictive modalities, inflating demand for neuromodulation and non-opioid analgesics. Medicaid expansion in additional U.S. states during 2025 further widens patient pools for comprehensive pain management programs.
Europe displays balanced maturation; Western states sustain incremental gains while Eastern markets accelerate device adoption under EU cohesion funding. The European Medicines Agency's rolling review procedures shortened average approval times for biosimilars and novel analgesics by 15% in 2025. National health technology assessment bodies increasingly recognize quality-of-life outcomes, prompting broader reimbursement for validated neuromodulation indications.
Asia-Pacific delivers the fastest regional CAGR at 10.55% through 2031. China's Healthy 2030 blueprint earmarks chronic pain as a priority, enabling tier-two hospitals to establish specialty pain clinics. India's telemedicine guidelines passed in 2025 legitimize e-prescriptions of non-schedule drugs, spurring digital consultation platforms. However, uneven insurance penetration and fragmented provider markets still limit uptake of high-cost implantables, constraining absolute market size relative to demographic potential.