A Randomized Placebo-Controlled Trial of Efficacy and Safety: Drug-Free Gel Containing Ultra-Deformable Phospholipid Vesicles (TDT 064) in Osteoarthritic Knees.

IF 1.9 Q2 ORTHOPEDICS Clinical Medicine Insights. Arthritis and Musculoskeletal Disorders Pub Date : 2021-07-28 eCollection Date: 2021-01-01 DOI:10.1177/11795441211031338
Varah Yuenyongviwat, Khanin Iamthanaporn, Pakjai Tuntarattanapong, Theerawit Hongnaparak, Boonsin Tangtrakulwanich
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Abstract

Background: There are a number of topical agents that are used for treatment of knee osteoarthritis. Drug-free gels, containing ultra-deformable phospholipid vesicles (TDT 064) are one such topical therapy, which have been stated to act as a bio lubricant. However, the evidence of TDT 064 in treatment of knee osteoarthritis is limited. Hence, the aim of this study was to evaluate the efficacy of pain control as a primary outcome and safety of TDT 064 compared with a topical placebo.

Methods: Sixty-four patients with primary osteoarthritis, with radiographic showing Kellgren and Lawrence classification grade II to III, were randomized into 2 groups. In the first group of 32 patients TDT 064 was used as topical agent, whilst in the second group of 32 patients a placebo identical in appearance was used instead. The verbal numerical rating scale (VNRS) was used for recording pain levels, Self-reported Knee Injury and Osteoarthritis Outcome Scores (KOOS) as well as amounts of rescue medication were also recorded. The data were recorded at the start of the study, and then at follow-up appointments of 14 days, 6 weeks, and 3 months.

Results: The mean VNRS for pain in both groups were significantly improved, when compared to the start of treatment (P < .0001); however, there were no differences between groups at any follow up visit. KOOS in all subscales were not significantly different between both groups at baseline and at the end of treatment. However, the average amount of NSAIDs in the TDT 064 group was 26.39 ± 22.11 tabs, which was significantly lower than the control group; which used an average 37.03 ± 19.22 tabs in 3 months (P = .047).

Conclusions: There were no differences in the VNRS for pain and KOOS scores between the active and placebo groups. Although, TDT 064 could decrease usage of rescue medication the difference with use of a placebo was minimal. Further, larger trials would also be beneficial to demonstrate any differences between TDT 064 and a placebo.

Trial registration: TCTR, TCTR 20190302001. Registered 1 March, 2019: http://www.clinicaltrials.in.th.

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一项疗效和安全性的随机安慰剂对照试验:含有超可变形磷脂囊泡(TDT 064)的无药凝胶治疗骨关节炎膝关节。
背景:有许多局部药物用于治疗膝骨关节炎。含有超可变形磷脂囊泡(TDT 064)的无药凝胶是一种这样的局部治疗方法,它被认为是一种生物润滑剂。然而,TDT 064治疗膝骨关节炎的证据有限。因此,本研究的目的是评估作为主要结局的疼痛控制的有效性以及TDT 064与外用安慰剂的安全性。方法:64例影像学表现为Kellgren和Lawrence分级II至III级的原发性骨关节炎患者随机分为两组。在第一组32名患者中,使用TDT 064作为局部用药,而在第二组32名患者中,使用外观相同的安慰剂代替。采用口头数字评定量表(VNRS)记录疼痛程度,并记录自述膝关节损伤和骨关节炎结局评分(kos)以及抢救用药数量。在研究开始时记录数据,然后在随访14天、6周和3个月时记录数据。结果:两组患者疼痛的平均VNRS较治疗前均有显著改善(P = 0.047)。结论:活性组和安慰剂组在疼痛和kos评分的VNRS评分上无差异。虽然TDT 064可以减少救援药物的使用,但与使用安慰剂的差异很小。此外,更大规模的试验也将有利于证明TDT 064与安慰剂之间的任何差异。试验注册号:TCTR, TCTR 20190302001。2019年3月1日注册:http://www.clinicaltrials.in.th。
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来源期刊
CiteScore
4.40
自引率
0.00%
发文量
14
审稿时长
8 weeks
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