Univ Angers, POPS, SFR ICAT, Angers, F-49000, France.
Biostatistics and Methodology Department, Angers University Hospital, Angers, France.
Trials. 2024 Oct 3;25(1):654. doi: 10.1186/s13063-024-08476-0.
Urinary tract infections are common affections, especially for women. Difficult access to a general practitioner to obtain a prescription has led France to offer dispensing under protocol by community pharmacists. The primary objective of this study is to evaluate the effectiveness of a pharmacist care protocol provided to manage women with urinary tract infection symptoms. This objective will be assessed using the Acute Cystitis Symptom Score.
PharmaCyst' is an open-label, multicenter, controlled, cluster-randomized study conducted in the Loire region, France. Women aged between 18 and 65 years presenting to a pharmacy complaining of at least one symptom of an uncomplicated urinary tract infection present over the last 3 days (including burning pain during micturition, dysuria, pollakiuria, urgent urination) will be considered for inclusion. All patients will be contacted on day 3, 10, and month 3. A total of 480 patients need to be recruited for the 24 clusters participating in the research. The quantitative data will be described using means and standard deviations and compared using Student's t-test. The qualitative data will be described using numbers and percentages and compared using chi test (or Fisher's exact test if necessary). The primary and secondary outcomes analyses will consider the intention-to-treat population.
PharmaCyst' is the first clinical trial conducted in France only by community pharmacists. Its results could lead to an extension of the protocol.
The protocol has been approved by the French ethics committee on 2022/12/02 and is registered under the number 49RC22_0240 on ClinicalTrials.gov.
尿路感染是常见疾病,尤其是女性。由于难以获得全科医生的处方,法国允许社区药剂师根据方案配药。本研究的主要目的是评估为管理有尿路感染症状的女性而提供的药剂师护理方案的有效性。该目标将通过急性膀胱炎症状评分进行评估。
PharmaCyst' 是一项在法国卢瓦尔地区进行的开放标签、多中心、对照、集群随机研究。将考虑患有至少一种过去 3 天出现的(包括排尿时烧灼感、尿痛、尿频、尿急)简单尿路感染症状的 18 至 65 岁女性纳入研究。所有患者将在第 3、10 和第 3 个月时进行联系。共有 480 名患者需要纳入参与研究的 24 个集群。定量数据将使用均值和标准差进行描述,并使用学生 t 检验进行比较。定性数据将使用数字和百分比进行描述,并使用卡方检验(如果需要,则使用 Fisher 确切检验)进行比较。主要和次要结局分析将考虑意向治疗人群。
PharmaCyst' 是法国首次仅由社区药剂师进行的临床试验。其结果可能导致方案的扩展。
该方案已于 2022 年 12 月 2 日获得法国伦理委员会的批准,并在 ClinicalTrials.gov 上注册为编号 49RC22_0240。