PMID- 30851540 OWN - NLM STAT- MEDLINE DCOM- 20190617 LR - 20200106 IS - 2299-5684 (Electronic) IS - 1734-1140 (Linking) VI - 71 IP - 2 DP - 2019 Apr TI - A systematic review and meta-analysis of oxaceprol in the management of osteoarthritis: An evidence from randomized parallel-group controlled trials. PG - 374-383 LID - S1734-1140(18)30545-0 [pii] LID - 10.1016/j.pharep.2018.12.010 [doi] AB - Oxaceprol, a derivative of l-proline, is an established drug for managing osteoarthritis (OA) with better safety profile than non-steroidal anti-inflammatory drugs (NSAIDs). This systematic review and meta-analysis, following Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) guidelines, evaluated the efficacy, safety and tolerability of oxaceprol in OA. Electronic databases for published and grey (unpublished) literature were searched to identify parallel-group randomized controlled trials (RCTs) evaluating the impact of oxaceprol in patients with OA. Risk of bias was assessed using the Cochrane collaboration's tool. A total of seven parallel-group RCTs involving 1087 participants were included in the systematic review. Meta-analysis, in Review Manager, demonstrated numerically greater/significant improvements compared to active control [diclofenac/ibuprofen]/placebo in pain and function of joint; similar improvement vs. active control in global treatment efficacy; no difference/significant difference vs. active control/placebo in NSAIDs as rescue medication. Treatment with oxaceprol showed numerically less adverse events (AEs) than active control (diclofenac: risk ratio [RR], 0.71; 95% confidence interval [CI], 0.45 to 1.11; p=0.14: ibuprofen: RR, 0.73; 95% CI, 0.30 to 1.78; p=0.49) and significantly fewer AEs compared to placebo (RR, 0.76; 95% CI, 0.63 to 0.92; p=0.004). Given the nature of small-to-moderate sample size and short duration of eligible studies, the available clinical evidence of oxaceprol in the management of OA is modest - though looks promising. New and better RCTs with larger sample size and longer follow-up are warranted to strengthen the use of oxaceprol in clinical setting for managing OA. CI - Copyright (c) 2018 Institute of Pharmacology, Polish Academy of Sciences. Published by Elsevier B.V. All rights reserved. FAU - Durg, Sharanbasappa AU - Durg S AD - Real World Evidence, Molecular Connections (P) Ltd., Basavanagudi, Bengaluru, India. Electronic address: sharanbasappa.d@molecularconnections.com. FAU - Lobo, Melita AU - Lobo M AD - Real World Evidence, Molecular Connections (P) Ltd., Basavanagudi, Bengaluru, India. FAU - Venkatachalam, Lakshmi AU - Venkatachalam L AD - Real World Evidence, Molecular Connections (P) Ltd., Basavanagudi, Bengaluru, India. FAU - Rao, Guruprasad AU - Rao G AD - Real World Evidence, Molecular Connections (P) Ltd., Basavanagudi, Bengaluru, India. FAU - Bhate, Jignesh AU - Bhate J AD - Real World Evidence, Molecular Connections (P) Ltd., Basavanagudi, Bengaluru, India. LA - eng PT - Comparative Study PT - Journal Article PT - Meta-Analysis PT - Systematic Review DEP - 20181226 PL - Switzerland TA - Pharmacol Rep JT - Pharmacological reports : PR JID - 101234999 RN - 0 (Anti-Inflammatory Agents, Non-Steroidal) RN - 0 (Antirheumatic Agents) RN - 144O8QL0L1 (Diclofenac) RN - Q0XV76B96L (oxaceprol) RN - RMB44WO89X (Hydroxyproline) RN - WK2XYI10QM (Ibuprofen) SB - IM MH - Anti-Inflammatory Agents, Non-Steroidal/administration & dosage/adverse effects MH - Antirheumatic Agents/adverse effects/*therapeutic use MH - Diclofenac/administration & dosage/adverse effects MH - Humans MH - Hydroxyproline/adverse effects/*therapeutic use MH - Ibuprofen/administration & dosage/adverse effects MH - Osteoarthritis/*drug therapy/physiopathology MH - Randomized Controlled Trials as Topic MH - Sample Size OTO - NOTNLM OT - Meta-analysis OT - Osteoarthritis OT - Oxaceprol OT - Safety OT - Systematic review EDAT- 2019/03/10 06:00 MHDA- 2019/06/18 06:00 CRDT- 2019/03/10 06:00 PHST- 2018/09/06 00:00 [received] PHST- 2018/11/10 00:00 [revised] PHST- 2018/12/21 00:00 [accepted] PHST- 2019/03/10 06:00 [pubmed] PHST- 2019/06/18 06:00 [medline] PHST- 2019/03/10 06:00 [entrez] AID - S1734-1140(18)30545-0 [pii] AID - 10.1016/j.pharep.2018.12.010 [doi] PST - ppublish SO - Pharmacol Rep. 2019 Apr;71(2):374-383. doi: 10.1016/j.pharep.2018.12.010. Epub 2018 Dec 26.