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Efficacy of Surgical Joint Denervation in Painful Digital Osteoarthritis

Efficacy of Surgical Joint Denervation in Painful Digital Osteoarthritis

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05378841
Acronym
DECAD
Enrollment
19
Registered
2022-05-18
Start date
2023-06-05
Completion date
2026-06-15
Last updated
2025-07-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osteoarthritis Hand

Keywords

Digital osteoarthritis, Surgical joint dernervation

Brief summary

Digital osteoarthritis is the second localization of symptomatic osteoarthritis, after the knee. Its cardinal symptoms are particularly intense pain and functional impairment in the case of the erosive form. There is currently no etiological treatment for osteoarthritis. Symptomatic treatments have a modest efficacy, which justifies the search for new treatments. The surgical options are arthrodesis or prosthesis, invasive techniques potentially sources of complications, and finally proposed infrequently given the prevalence of digital osteoarthritis. DECAD is a prospective phase II trial aimed at evaluating the efficacy of surgical joint denervation in painful digital osteoarthritis.

Detailed description

Osteoarthritis is the most common joint pathology of the musculoskeletal system. It affects 6 million French people and constitutes a public health problem. Osteoarthritis of the hands or digitalis is the second localization of symptomatic osteoarthritis, after the knee. Its main risk factors are female sex, age, genetic factors, and obesity. Osteoarthritis combines articular cartilage degradation, synovial inflammation, subchondral bone remodeling and osteophyte development. Its cardinal symptoms are pain and functional impairment (at a level sometimes close to inflammatory rheumatism such as rheumatoid arthritis), particularly intense in the case of the erosive form. There is also local joint inflammation associated with pain. Pain in osteoarthritis is a complex phenomenon involving joint tissues other than cartilage, a tissue that is not innervated (subchondral bone, joint capsule, synovial membrane). There is currently no etiological treatment for osteoarthritis. Symptomatic treatments have a modest efficacy, which justifies the search for new treatments. The surgical options are arthrodesis or prosthesis, invasive techniques potentially sources of complications, and finally proposed infrequently given the prevalence of digital osteoarthritis. The only current conservative surgical solution that can be proposed for intractable painful proximal interphalangeal joint (PIPJ) osteoarthritis is denervation. This technique consists of cutting the nerve branches intended for the PIPJ in order to directly interrupt the pain pathways. It reduces pain by 80% after 5 years, without loss of mobility. There are only 4 published series reporting the results of this technique (2-3). These were retrospective case series with a low level of evidence. The patient satisfaction rate reached 90%, with transient paresthesias as the only reported complication. The mechanism of action for the effectiveness of this intervention has never been studied. Our hypothesis is that denervation of the PIP has clinical efficacy in painful digital osteoarthritis refractory to usual treatments, and that it would have a structural effect that can be objectified on MRI. The results of this pilot study will make it possible to construct a prospective randomized study.

Interventions

PROCEDURESurgical Denervation

This is an outpatient procedure performed under local anesthesia (depending on the anesthesiologist's decision), which lasts about 30 minutes.

Sponsors

Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥ 18 years * Patients with symptomatic digital osteoarthritis according to the criteria of the American College of Rheumatology * 1 painful PIP joint (Analog digital scale ≥ 4/10) for more than 3 months * having failed the usual medical treatment for a minimum of 3 months (level 1 analgesics, NSAIDs, infiltrations) * Signature of informed consent * patient affiliated to a social security scheme * knowing how to read French (for the questionnaires)

Exclusion criteria

* digital osteoarthritis secondary to other known causes (eg gout, reactive arthritis, RA, psoriatic arthritis, spondyloarthropathies, septic arthritis) * anesthetic contraindications to surgery or to performing an MRI * Existence of a pain syndrome in the upper limbs, which would interfere with the assessment of AD. * Fibromyalgia * Use of oral, intramuscular or intra-articular or intravenous corticosteroids, immunosuppressants (methotrexate, sulfasalazine, leflunomide, biomedicines), hyaluronic acid infiltration in the finger joints in the previous month * Introduction of a new treatment for osteoarthritis of the hand in the previous month, including physiotherapy and fitting of a new finger orthosis. * History of denervation of the proximal interphalangeal joint (PIP) * Patient under legal protection (guardianship or curatorship) and patient deprived of liberty * Patient under AME * Participation in another interventional research involving the human person or period of exclusion at the end of a previous research involving the human person.

Design outcomes

Primary

MeasureTime frameDescription
Success of the intervention at 3 months3 monthsSuccess of the intervention at 3 months, defined by a reduction in pain of at least 2 points compared to the measurement at inclusion, with the numerical painscale (from 0 to 10) for the operate finger

Secondary

MeasureTime frameDescription
Pain at 6 months6 monthsAssessement with Numerical pain scale of the operated finger and the operated hand (from 0 to 10)
Quality of life at 6 months : Score quick-DASH6 monthsCalculation of score by quick-DASH questionnary: main functional and quality of life and function score used in hand surgery
Quality of life at 6 months : Score AUSCAN6 monthsCalculation of score by AUSCAN questionnary (Australian/Canadian Osteo Arthritis Hand Index, self-administered questionnaire validated in AD measuring pain, function and stiffness)
Grip strength at 6 months6 monthsGrip strength measured by JAMAR hydraulic dynamometer to assess the impact of pain on function
PGI-C Score at 6 months6 monthsCalculation of score on PGI-C scale (Patient Global Impressions scale-Change, assesses the perception of a change induced by the treatment) to assess patient satisfaction

Countries

France

Contacts

Primary ContactAdeline CAMBON-BINDER, MD PhD
adeline.cambonbinder@aphp.fr685573795
Backup ContactJérémie SELLAM
jeremie.sellam@aphp.fr+ 33 1 49 28 25 20

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026