Rebecca M Lane, Laurence J Egan, Brian E McGuire, Declan P McKernan, Siobhain M O'Mahony, David P Finn
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We will search CENTRAL, MEDLINE, PubMed, EMBASE, and Web of Science databases, as well as the WHO International Clinical Trials Registry Platform and ClinicalTrials.gov Trials Registries, together with reference checking and citation searching, following PRISMA guidelines. Our objectives are to evaluate the benefits and harms of pharmacological modulation of the ECS for visceral abdominal pain in patients with IBD or IBS, compared to placebo or other interventions. The primary outcomes will be the proportion of people with (a) at least a 30% reduction and (b) at least a 50% reduction in pain. Secondary outcomes will include any change in pain intensity, physical and emotional functioning, fatigue and sleep measures, quality of life, gastrointestinal disease or symptom severity, and adverse effects. We will assess risk of bias in the RCTs using the Cochrane Risk of Bias 2 tool. Where there are sufficient data that are directly comparable, we will conduct meta-analyses of the results for each outcome. We will use the GRADEpro GDT tool to assess certainty of evidence for each outcome. This review will synthesise the available evidence regarding all types of ECS modulation for the treatment of visceral abdominal pain and its related comorbidities in IBS and IBD patients.</p>","PeriodicalId":73254,"journal":{"name":"HRB open research","volume":"8 ","pages":"40"},"PeriodicalIF":0.0000,"publicationDate":"2025-07-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12375179/pdf/","citationCount":"0","resultStr":"{\"title\":\"Endocannabinoid system modulation for visceral abdominal pain in inflammatory bowel disease and irritable bowel syndrome: A protocol for systematic review and meta-analysis.\",\"authors\":\"Rebecca M Lane, Laurence J Egan, Brian E McGuire, Declan P McKernan, Siobhain M O'Mahony, David P Finn\",\"doi\":\"10.12688/hrbopenres.14082.2\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Visceral Pain is a common debilitating symptom of inflammatory bowel disease (IBD) and irritable bowel syndrome (IBS). 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Our objectives are to evaluate the benefits and harms of pharmacological modulation of the ECS for visceral abdominal pain in patients with IBD or IBS, compared to placebo or other interventions. The primary outcomes will be the proportion of people with (a) at least a 30% reduction and (b) at least a 50% reduction in pain. Secondary outcomes will include any change in pain intensity, physical and emotional functioning, fatigue and sleep measures, quality of life, gastrointestinal disease or symptom severity, and adverse effects. We will assess risk of bias in the RCTs using the Cochrane Risk of Bias 2 tool. Where there are sufficient data that are directly comparable, we will conduct meta-analyses of the results for each outcome. We will use the GRADEpro GDT tool to assess certainty of evidence for each outcome. 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引用次数: 0
摘要
内脏疼痛是炎症性肠病(IBD)和肠易激综合征(IBS)的常见衰弱症状。内源性大麻素系统(ECS)是减轻内脏疼痛的主要目标,因为它在胃肠道生理学和疼痛中都起着重要作用。我们将对针对IBD和IBS患者的大麻、大麻素、基于大麻的药物(CBM)和其他ECS调节剂的随机对照试验(rct)进行系统评价,比较任何大麻制剂、任何大麻素、CBM或其他ECS药理学调节剂(任何剂量、任何给药途径)与任何对照(安慰剂、或药理学/心理/饮食干预)。我们将检索CENTRAL、MEDLINE、PubMed、EMBASE和Web of Science数据库,以及WHO国际临床试验注册平台和ClinicalTrials.gov试验注册,并按照PRISMA指南进行参考检查和引文检索。我们的目的是评估与安慰剂或其他干预措施相比,药物调节ECS治疗IBD或IBS患者内脏性腹痛的利与弊。主要结局将是(a)至少减轻30%疼痛和(b)至少减轻50%疼痛的患者比例。次要结局将包括疼痛强度、身体和情绪功能、疲劳和睡眠测量、生活质量、胃肠道疾病或症状严重程度以及不良反应的任何变化。我们将使用Cochrane risk of bias 2工具评估随机对照试验的偏倚风险。如果有足够的数据可以直接比较,我们将对每个结果进行荟萃分析。我们将使用GRADEpro GDT工具来评估每个结果的证据确定性。本综述将综合所有类型的ECS调节治疗IBS和IBD患者内脏性腹痛及其相关合并症的现有证据。
Endocannabinoid system modulation for visceral abdominal pain in inflammatory bowel disease and irritable bowel syndrome: A protocol for systematic review and meta-analysis.
Visceral Pain is a common debilitating symptom of inflammatory bowel disease (IBD) and irritable bowel syndrome (IBS). The endocannabinoid system (ECS) is a prime target for alleviation of visceral pain, given its important role in both gastrointestinal physiology and pain. We will conduct a systematic review of randomised controlled trials (RCTs) of cannabis, cannabinoids, cannabis-based medicines (CBMs), and other ECS modulators for patients with IBD and IBS, comparing any preparation of cannabis, any cannabinoid, CBM, or other pharmacological modulator of the ECS (any dose, by any route of administration), with any control (placebo, or pharmacological / psychological / dietary intervention). We will search CENTRAL, MEDLINE, PubMed, EMBASE, and Web of Science databases, as well as the WHO International Clinical Trials Registry Platform and ClinicalTrials.gov Trials Registries, together with reference checking and citation searching, following PRISMA guidelines. Our objectives are to evaluate the benefits and harms of pharmacological modulation of the ECS for visceral abdominal pain in patients with IBD or IBS, compared to placebo or other interventions. The primary outcomes will be the proportion of people with (a) at least a 30% reduction and (b) at least a 50% reduction in pain. Secondary outcomes will include any change in pain intensity, physical and emotional functioning, fatigue and sleep measures, quality of life, gastrointestinal disease or symptom severity, and adverse effects. We will assess risk of bias in the RCTs using the Cochrane Risk of Bias 2 tool. Where there are sufficient data that are directly comparable, we will conduct meta-analyses of the results for each outcome. We will use the GRADEpro GDT tool to assess certainty of evidence for each outcome. This review will synthesise the available evidence regarding all types of ECS modulation for the treatment of visceral abdominal pain and its related comorbidities in IBS and IBD patients.