Table 1

Summarised study characteristics, stratified by intervention class

InterventionNumber of referencesNumber of participants (ITT)Number of references with data for the outcome domainHand OA target
PainFunctionPGAHRQoLGrip strengthAE withdrawalsSAEFingers onlyThumb onlyBoth thumb and fingers
Capsaicin2732100022002
Topical NSAID916387633566225
Topical salicylate21312000010200
Glucosamine1501000000001
Galactosaminoglycuronglycan sulfate1241000000100
Chondroitin sulfate33511210122111
Unsaponifiables*12610000000001
Paracetamol42144000010004
Oral NSAID11217210321365416
Salicylate injection1401100011010
Prolotherapy2872100122011
Intra-articular platelet-rich plasma2782200110020
Intra-articular hyaluronate11766106015760110
Intra-articular glucocorticoids11734118116871100
Perineural glucocorticoids1501101110001
Radiation1561111011001
Oral glucocorticoids32453221132102
PDE4 inhibitors1301111011100
Colchicine1641100111001
SNRI1651100010001
Antiepileptics1651100010001
Cannabidiol1771000000001
Bisphosphonates2782210122101
Hydroxychloroquine67476322265204
Methotrexate1641110010100
TNF inhibitor42714210144103
IL-1 inhibitor43952222124004
IL-6 inhibitor1911110011100
GM-CSF inhibitor1441100011100
Total72760964401712215145171936
  • Traffic light colours indicate completeness of reporting (0–33% red, 34–66% yellow, 67–100% green).

  • *The trial reported overall data and were therefore included; however, no arm-based data were available.

  • .AE, adverse event; GM-CSF, granulocyte-macrophage colony-stimulating factor; HRQoL, health-related quality of life; IL, interleukin; ITT, intention-to-treat; NSAID, non-steroidal anti-inflammatory drug; OA, osteoarthritis; PDE4, phosphodiesterase-4; PGA, patient global assessment; SAE, serious adverse event; SNRI, selective norepinephrine reuptake inhibitors; TNF, tumour necrosis factor.