Table 1

Summary of characteristics of included studies

TotalChondroitinGlucosamineChondroitin + glucosamineParacetamolNSAIDsTopical NSAIDsPEMFAcupunctureIACSIAHAJoint lavage
No. of trials2151321576320191710364
No. of participants41 392254628691055234518 6174400100227236124796427
Median age (IQR), years62.2 (60.0 to 64.2)63.0 (60.0 to 65.0)61.7 (58.3 to 64.5)58.6 (56.7 to 67.6)62.6 (61.9 to 64.1)61.6 (60.1 to 62.6)63.2 (61.5 to 65.3)61.6 (59.6 to 63.9)64.8 (62.8 to 67.0)64.9 (63.2 to 66.0)62.6 (59.5 to 64.6)57.1 (54.0 to 60.7)
Median percentage of women (IQR), %65.8 (60.0 to 72.8)65.9 (55.8 to 72.1)64.4 (60.3 to 81.3)82.5 (70.8 to 88.2)66.9 (64.5 to 74.8)66.8 (62.9 to 71.0)65.0 (61.6 to 74.5)71.6 (61.8 to 90.2)65.0 (61.0 to 69.1)67.5 (61.7 to 71.4)61.0 (51.3 to 70.1)58.7 (29.9 to 67.2)
Median years of symptom (IQR)6.8 (5.0 to 8.7)6.6 (6.4 to 6.8)9.2 (7.1 to 12.0)7.8 (5.5 to 10.0)7.8 (5.3 to 8.7)7.2 (5.4 to 8.8)7.4 (3.6 to 10.8)6.0 (3.6 to 8.2)7.0 (6.5 to 7.5)7.6 (6.0 to 9.3)4.8 (2.7 to 6.2)10.4 (–)
Pooled baseline pain (95% CI) in 0–100 scale54.8 (50.8 to 58.9)57.2 (48.9 to 65.5)51.4 (39.8 to 63.0)42.8 (25.8 to 59.9)49.7 (33.9 to 65.5)56.1 (46.8 to 65.3)59.7 (53.8 to 65.5)55.4 (47.3 to 63.5)41.4 (34.8 to 47.9)60.0 (46.6 to 73.3)56.4 (52.0 to 60.8)65.4 (43.3 to 87.4)
Median duration of trial (IQR), weeks12 (4 to 13)26 (13 to 52)12 (7 to 24)16 (12 to 24)6 (6 to 12)6 (4 to 12)4 (2 to 12)6 (3 to 10)9 (4 to 13)9 (3 to 12)16 (9 to 26)52 (38 to 78)
Quality of included studies
 Randomisation12291532241912124184
 Allocation concealment968113118151292143
 Blinding to participants199132057611817169303
 Intent to treat analysis141913274519796222
  • IACS, intra-articular corticosteroid; IAHA, intra-articular hyaluronic acid; NSAIDs, non-steroidal anti-inflammatory drugs; PEMF, pulsed electromagnetic field therapy.