Vance Thompson Vision, Sioux Falls, SD, USA.
University of South Dakota, Sanford School of Medicine, Sioux Falls, SD, USA.
Transl Vis Sci Technol. 2023 Mar 1;12(3):7. doi: 10.1167/tvst.12.3.7.
Evaluation of safety and efficacy of topical ocular SAF312 (Libvatrep) in post-photorefractive keratectomy (PRK) pain.
In this placebo (vehicle)-controlled, participant- and investigator-masked study, 40 participants were randomized (1:1) to two treatment sequences in a bilateral PRK crossover design (SAF312 2.5% followed by vehicle [or vice versa], one eye drop, four times daily for 72 hours after PRK). Primary endpoints were visual analog scale (VAS) pain scores at 6 hours after first drop of study drug and average VAS scores over 0 to 12 hours postoperatively. Secondary endpoints included postoperative oral rescue medication (ORM) use and adverse events (AEs).
All 40 participants completed the study. Both primary endpoints were met; mean difference in VAS pain scores between SAF312- and vehicle-treated eyes was -11.13 (P = 0.005, -25%) at 6 hours postoperatively and -8.56 (P = 0.017, -22%) over 0 to 12 hours. Mean VAS pain scores with SAF312 were consistently lower than with vehicle from 1 hour postoperatively up to 30 hours (P ≤ 0.10 observed in 8/11 time points). Less ORM was taken with SAF312 up to 0 to 72 hours postoperatively, with a trend of fewer participants taking ORM at 0 to 24 hours postoperatively with SAF312 versus vehicle. No serious AEs were reported. All ocular AEs were mild and transient, and none were drug related. SAF312-treated eyes showed no delay in wound healing and had a lower grade 4 conjunctival hyperemia 24 hours postoperatively versus vehicle-treated eyes.
SAF312 was well tolerated and effective in reducing ocular pain post-PRK.
Topical SAF312 presents a new therapeutic option for patients undergoing PRK.
评估局部眼部 SAF312(利伐曲普)在光折射性角膜切削术(PRK)后疼痛中的安全性和疗效。
在这项安慰剂(载体)对照、参与者和研究者盲法研究中,40 名参与者按照双侧 PRK 交叉设计(SAF312 2.5% 后接载体[或反之],单次滴眼,每日 4 次,共 72 小时)随机(1:1)分为两组。主要终点为首次滴药后 6 小时的视觉模拟评分(VAS)疼痛评分和术后 0 至 12 小时的平均 VAS 评分。次要终点包括术后口服解救药物(ORM)使用和不良事件(AE)。
所有 40 名参与者均完成了研究。两个主要终点均达到;SAF312 治疗眼与载体治疗眼的 VAS 疼痛评分差异在术后 6 小时为-11.13(P = 0.005,-25%),在术后 0 至 12 小时为-8.56(P = 0.017,-22%)。SAF312 治疗后的平均 VAS 疼痛评分从术后 1 小时至 30 小时持续低于载体治疗(8/11 个时间点观察到 P ≤ 0.10)。SAF312 治疗至术后 0 至 72 小时的 ORM 用量较少,与载体治疗相比,SAF312 治疗至术后 0 至 24 小时的参与者中,使用 ORM 的人数呈减少趋势。未报告严重 AE。所有眼部 AE 均为轻度和一过性,且均与药物无关。SAF312 治疗的眼睛在术后 24 小时未见伤口愈合延迟,且 4 级结膜充血程度低于载体治疗的眼睛。
SAF312 耐受性良好,能有效减轻 PRK 术后眼部疼痛。
这是一篇医学论文的摘要,主要内容是评估一种名为 SAF312 的局部眼部药物在光折射性角膜切削术后疼痛中的安全性和疗效。研究采用了安慰剂对照、参与者和研究者盲法的设计,结果表明 SAF312 能有效减轻术后疼痛,且耐受性良好。