CTIS2023-507541-29-00进行中(未招募)1 期
EFFICACY AND SAFETY OF CROMOGLYCATE AS A NEW SYMPTOMATIC TREATMENT IN PATIENTS WITH MULTIPLE SCLEROSIS - ICI21/00022
Fundacion Para La Investigacion Biomedica Del Hospital Clinico San Carlos0 个研究点目标入组 120 人开始时间: 2023年8月30日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 120
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 64(—)
- 性别
- All
入选标准
- •Age between 18 and 60 years., Diagnosis of multiple sclerosis according to the 2017 McDonald criteria, with more than 6 months of follow-up and clinically stable (without flare-ups or new lesions) in the last 6 months., EDSS between 1.0 and 6.5 points., Presence of moderate fatigue for at least 6 months (defined by a score on the MFIS scale = 33 points) and urinary dysfunction (defined by 2 points or more on the ABSST Test).
排除标准
- •Inability to understand or sign the informed consent., Hypersensitivity to sodium cromoglycate or to any of the excipients (microcrytalline cellulose)., Concomitant pathologies of the CNS or diseases that, in the opinion of the investigator, may alter the control of micturition., Patients with permanent urinary catheters., Severe renal or hepatic impairment, history of myocardial infarction, or other clinically significant medical problems that, in the opinion of the investigators, may expose the patient to undue risk or harm, or render the patient unable to complete the study., Abnormal results on baseline blood tests, defined as: serum alanine transaminase or aspartate transaminase levels greater than five times the upper limit of normal, serum creatinine level greater than 1.5 mg/dL, or estimated glomerular filtration rate less than 60 mL /min/1.73 m2., Change in disease-modifying therapy in the last 3 months., Change in symptomatic treatment of fatigue and/or urinary incontinence in the last 3 months., Pregnant or lactating women., Inability to perform MRI (claustrophobia, pacemakers, metal implants) or known allergy to gadolinium.
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