Clinical and experimental rheumatology · 2025
Three-year follow-up from a randomised controlled trial of a single intra-articular polyacrylamide hydrogel injection in subjects with knee osteoarthritis.
СтатьяРандомизированное исследованиеНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Bliddal Henning, Beier Jannie, Hartkopp Andreas, Conaghan Philip G, Henriksen Marius
Аннотация
OBJECTIVES: A randomised controlled trial demonstrated comparable efficacy and safety of a single 6 mL intra-articular (IA) injection of 2.5% polyacrylamide hydrogel (2.5% iPAAG) versus hyaluronic acid (HA) over one year in adults with moderate-to-severe knee osteoarthritis (OA). This study evaluated the long-term effectiveness and safety of 2.5% iPAAG.
METHODS: This 3-year extension of a randomised controlled trial (RCT) (ClinicalTrials.gov Identifier: NCT04045431) followed participants who received a single 6 mL IA injection of 2.5% iPAAG. Outcomes included changes from baseline to year 3 in WOMAC pain, stiffness, and physical function subscales (0-100 scale) and patient global assessment (PGA) of OA impact. Safety was assessed up to year 3.
RESULTS: A total of 119 participants received IA 2.5% iPAAG. After one year, 91 participants (44 females) entered the extension study, and 75 completed 3-years of follow-up. At year 3, the mean change in WOMAC pain was -13.1 (95% CI: -17.9 to -8.4; p<0.0001). Between the 1-year and 3-year visits, fifty adverse events (AEs) were reported by 36 participants (29.8%), none of which were assessed as related to 2.5% iPAAG.
CONCLUSIONS: A single 6 mL IA injection of 2.5% iPAAG appears to be safe and effective in providing sustained symptom relief for up to 3 years in individuals with knee OA.
METHODS: This 3-year extension of a randomised controlled trial (RCT) (ClinicalTrials.gov Identifier: NCT04045431) followed participants who received a single 6 mL IA injection of 2.5% iPAAG. Outcomes included changes from baseline to year 3 in WOMAC pain, stiffness, and physical function subscales (0-100 scale) and patient global assessment (PGA) of OA impact. Safety was assessed up to year 3.
RESULTS: A total of 119 participants received IA 2.5% iPAAG. After one year, 91 participants (44 females) entered the extension study, and 75 completed 3-years of follow-up. At year 3, the mean change in WOMAC pain was -13.1 (95% CI: -17.9 to -8.4; p<0.0001). Between the 1-year and 3-year visits, fifty adverse events (AEs) were reported by 36 participants (29.8%), none of which were assessed as related to 2.5% iPAAG.
CONCLUSIONS: A single 6 mL IA injection of 2.5% iPAAG appears to be safe and effective in providing sustained symptom relief for up to 3 years in individuals with knee OA.