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PRECISE - 普瑞巴林联合常规治疗坐骨神经痛:一项随机对照试验的研究方案。

PRECISE - pregabalin in addition to usual care for sciatica: study protocol for a randomised controlled trial.

机构信息

The George Institute for Global Health and Sydney Medical School, University of Sydney, PO Box M201, Missenden Rd, Camperdown, Sydney, NSW 2050, Australia.

出版信息

Trials. 2013 Jul 11;14:213. doi: 10.1186/1745-6215-14-213.

Abstract

BACKGROUND

Sciatica is a type of neuropathic pain that is characterised by pain radiating into the leg. It is often accompanied by low back pain and neurological deficits in the lower limb. While this condition may cause significant suffering for the individual, the lack of evidence supporting effective treatments for sciatica makes clinical management difficult. Our objectives are to determine the efficacy of pregabalin on reducing leg pain intensity and its cost-effectiveness in patients with sciatica.

METHODS/DESIGN: PRECISE is a prospectively registered, double-blind, randomised placebo-controlled trial of pregabalin compared to placebo, in addition to usual care. Inclusion criteria include moderate to severe leg pain below the knee with evidence of nerve root/spinal nerve involvement. Participants will be randomised to receive either pregabalin with usual care (n = 102) or placebo with usual care (n = 102) for 8 weeks. The medicine dosage will be titrated up to the participant's optimal dose, to a maximum 600 mg per day. Follow up consultations will monitor individual progress, tolerability and adverse events. Usual care, if deemed appropriate by the study doctor, may include a referral for physical or manual therapy and/or prescription of analgesic medication. Participants, doctors and researchers collecting participant data will be blinded to treatment allocation. Participants will be assessed at baseline and at weeks 2, 4, 8, 12, 26 and 52. The primary outcome will determine the efficacy of pregabalin in reducing leg pain intensity. Secondary outcomes will include back pain intensity, disability and quality of life. Data analysis will be blinded and by intention-to-treat. A parallel economic evaluation will be conducted from health sector and societal perspectives.

DISCUSSION

This study will establish the efficacy of pregabalin in reducing leg pain intensity in patients with sciatica and provide important information regarding the effect of pregabalin treatment on disability and quality of life. The impact of this research may allow the future development of a cost-effective conservative treatment strategy for patients with sciatica.

TRIAL REGISTRATION

ClinicalTrial.gov, ACTRN 12613000530729.

摘要

背景

坐骨神经痛是一种神经病理性疼痛,其特征是腿部放射性疼痛。它通常伴有腰痛和下肢神经功能缺损。虽然这种情况可能会给个人带来极大的痛苦,但缺乏支持坐骨神经痛有效治疗的证据使得临床管理变得困难。我们的目标是确定普瑞巴林在减轻腿部疼痛强度方面的疗效及其在坐骨神经痛患者中的成本效益。

方法/设计:PRECISE 是一项前瞻性注册、双盲、随机安慰剂对照试验,比较普瑞巴林与安慰剂,以及常规护理。纳入标准包括膝关节以下中度至重度腿部疼痛,有神经根/脊神经根受累的证据。参与者将被随机分配接受普瑞巴林加常规护理(n = 102)或安慰剂加常规护理(n = 102)治疗 8 周。药物剂量将滴定至参与者的最佳剂量,最大剂量为每天 600 毫克。随访咨询将监测个体进展、耐受性和不良事件。如果研究医生认为合适,常规护理可能包括转介进行物理或手动治疗和/或开具镇痛药物。参与者、医生和收集参与者数据的研究人员将对治疗分配进行盲法。参与者将在基线和第 2、4、8、12、26 和 52 周进行评估。主要结局将确定普瑞巴林减轻腿部疼痛强度的疗效。次要结局包括腰痛强度、残疾和生活质量。数据分析将进行盲法和意向治疗。将从卫生部门和社会角度进行平行的经济评估。

讨论

这项研究将确定普瑞巴林在减轻坐骨神经痛患者腿部疼痛强度方面的疗效,并提供关于普瑞巴林治疗对残疾和生活质量影响的重要信息。这项研究的结果可能允许为坐骨神经痛患者制定未来具有成本效益的保守治疗策略。

试验注册

ClinicalTrials.gov,ACTRN 12613000530729。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6669/3711833/2afafa22ec56/1745-6215-14-213-1.jpg

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