Norfolk and Norwich University Hospital, UK.
Ann R Coll Surg Engl. 2022 Apr;104(4):274-279. doi: 10.1308/rcsann.2021.0163. Epub 2021 Nov 25.
Rubber band ligation (RBL) is a procedure commonly performed in colorectal clinics for internal haemorrhoids. Overall, 90% of patients experience pain following RBL. We aimed to complete a feasibility randomised control trial assessing the role of topical anaesthetic before RBL of internal haemorrhoids.
We performed a prospective, single-centre, single blinded, randomised (1:1) control feasibility trial. Patients presenting with symptomatic haemorrhoids suitable for banding were randomised to undergo the procedure with local anaesthetic or without (control). Pain scores and vasovagal symptoms were assessed at 0 minutes, 30 minutes, 4 hours and 72 hours after the procedure. Primary outcome measures were recruitment rate, participant retention rate and patient and surgeon acceptability. Secondary outcome measures were pain scores up to 72 hours, vasovagal episodes, new use of analgesia and adverse outcomes.
In total, 35 patients (18 topical anaesthetic, group A; 17 no anaesthetic gel, group B) were recruited. Mean recruitment rate was 11.7 participants per month. Thirty-three (94%) participants remained in the study until completion, with two patients lost to telephone follow-up. The treatment was acceptable for 35 (97%) eligible patients. One patient declined enrolment. The treatment was acceptable to all surgeons (100%). There was a significant difference in median pain scores of -2 (95% CI -4.0 to -1.0, =0.0006) at the 30-minute time point only. There was no significant difference in vasovagal symptoms (=0.10) or new analgesia use (=0.85).
We have shown that a phase III clinical trial is feasible for assessing the role of topical anaesthetic before RBL of internal haemorrhoids. We have demonstrated excellent patient recruitment and retention as well as patient and surgeon acceptability.
橡皮圈结扎(RBL)是肛肠诊所治疗内痔的常用方法。总体而言,90%的患者在 RBL 后会感到疼痛。我们旨在完成一项评估内痔 RBL 前局部麻醉作用的可行性随机对照试验。
我们进行了一项前瞻性、单中心、单盲、随机(1:1)对照可行性试验。对适合结扎的症状性内痔患者进行随机分组,一组在接受手术时使用局部麻醉(A 组),另一组不使用(B 组)。在手术结束后 0 分钟、30 分钟、4 小时和 72 小时评估疼痛评分和血管迷走神经症状。主要结局指标为招募率、参与者保留率以及患者和外科医生的可接受性。次要结局指标为 72 小时内的疼痛评分、血管迷走神经发作、新使用镇痛药和不良结局。
共招募 35 名患者(A 组 18 名接受局部麻醉,B 组 17 名未使用麻醉凝胶)。平均招募率为每月 11.7 名参与者。33 名(94%)参与者完成了研究,有 2 名患者因电话随访而失访。有 35 名(97%)符合条件的患者对治疗表示接受。有 1 名患者拒绝入组。所有外科医生(100%)都认为该治疗方法是可接受的。仅在 30 分钟时,两组间的疼痛评分中位数差异有统计学意义(-2,95%CI-4.0 至-1.0,=0.0006)。血管迷走神经症状(=0.10)或新使用镇痛药(=0.85)无显著差异。
我们已经证明,评估内痔 RBL 前局部麻醉作用的 III 期临床试验是可行的。我们已经证明了良好的患者招募和保留率以及患者和外科医生的可接受性。