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注册号: Registration number: |
ChiCTR2500095449 |
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最近更新日期: Date of Last Refreshed on: |
2025-01-07 15:55:50 |
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注册时间: Date of Registration: |
2025-01-07 00:00:00 |
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注册号状态: |
预注册 |
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Registration Status: |
Prospective registration |
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注册题目: |
司美格鲁肽对比二甲双胍治疗精神分裂症伴代谢综合征患者:一项随机开放对照研究 |
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Public title: |
Semaglutide versus metformin in patients with schizophrenia and metabolic syndrome: a randomized, open-controlled study |
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注册题目简写: |
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English Acronym: |
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研究课题的正式科学名称: |
司美格鲁肽对比二甲双胍治疗精神分裂症伴代谢综合征患者:一项随机开放对照研究 |
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Scientific title: |
Semaglutide versus metformin in patients with schizophrenia and metabolic syndrome: a randomized, open-controlled study |
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研究课题代号(代码): Study subject ID: |
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在二级注册机构或其它机构的注册号: The registration number of the Partner Registry or other register: |
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申请注册联系人: |
郑财济 |
研究负责人: |
郑财济 |
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Applicant: |
Zheng Caiji |
Study leader: |
Zheng Caiji |
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申请注册联系人电话: Applicant telephone: |
+86 13824322360 |
研究负责人电话:
Study leader's |
+86 755 82924215 |
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申请注册联系人传真 : Applicant Fax: |
研究负责人传真: Study leader's fax: |
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申请注册联系人电子邮件: Applicant E-mail: |
caijizheng@qq.com |
研究负责人电子邮件: Study leader's E-mail: |
caijizheng@qq.com |
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申请单位网址(自愿提供): Applicant website(voluntary supply): |
研究负责人网址(自愿提供): Study leader's website(voluntary supply): |
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申请注册联系人通讯地址: |
深圳市坪山区振碧路77号 |
研究负责人通讯地址: |
深圳市坪山区振碧路77号 |
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Applicant address: |
No.77 Zhenbi Road, Pingshan District, Shenzhen |
Study leader's address: |
No.77 Zhenbi Road, Pingshan District, Shenzhen |
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申请注册联系人邮政编码: Applicant postcode: |
研究负责人邮政编码: Study leader's postcode: |
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申请人所在单位: |
深圳市康宁医院 |
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Applicant's institution: |
Shenzhen Kangning Hospital |
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研究负责人所在单位: |
深圳市康宁医院 |
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Affiliation of the Leader: |
Shenzhen Kangning Hospital |
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是否获伦理委员会批准: |
是 |
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Approved by ethic committee: |
Yes |
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伦理委员会批件文号: Approved No. of ethic committee: |
2023-K035-01-1 |
伦理委员会批件附件: Approved file of Ethical Committee: |
查看附件View |
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批准本研究的伦理委员会名称: |
深圳市康宁医院医学伦理委员会 |
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Name of the ethic committee: |
Medical Ethics Committee of Shenzhen Kangning Hospital |
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伦理委员会批准日期: Date of approved by ethic committee: |
2024-06-14 00:00:00 | ||
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伦理委员会联系人: |
王琪 |
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Contact Name of the ethic committee: |
Wang Qi |
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伦理委员会联系地址: |
深圳市坪山区碧岭街道振碧路77号深圳市康宁医院坪山院区 |
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Contact Address of the ethic committee: |
Shenzhen Kangning Hospital, 77 Zhenbi Rd. Pingshan, Shenzhen |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 755 82926524 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
kangning_ethics@163.com |
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研究实施负责(组长)单位: |
深圳市康宁医院 |
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Primary sponsor: |
Shenzhen Kangning Hospital |
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研究实施负责(组长)单位地址: |
深圳市坪山区碧岭街道振碧路77号深圳市康宁医院坪山院区 |
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Primary sponsor's address: |
Shenzhen Kangning Hospital, 77 Zhenbi Rd. Pingshan, Shenzhen |
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试验主办单位(项目批准或申办者): Secondary sponsor: |
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经费或物资来源: |
司美格鲁肽对比二甲双胍治疗精神分裂症伴代谢综合征患者:一项随机开放对照研究 |
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Source(s) of funding: |
Research funds within the hospital |
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研究疾病: |
精神分裂症 |
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Target disease: |
Schizophrenia |
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研究疾病代码: |
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Target disease code: |
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研究类型: |
干预性研究 |
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Study type: |
Interventional study |
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研究所处阶段: |
其它 | ||||||||||||||||||||||
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Study phase: |
N/A |
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研究设计: |
随机平行对照 |
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Study design: |
Parallel |
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研究目的: |
目的开展司美格鲁肽对比二甲双胍治疗精神分裂症伴代谢综合征研究。精神疾病本身和抗精神病药物均会增加代谢综合征和糖尿病的风险,既往有研究已证明二甲双胍具有降低抗精神病药物引起体重增加报告,但是二甲双胍使用要求是每日规律服药,这对依从性不佳的精神疾病患者造成重大挑战。司美格鲁肽注射液作为一种每周一次的长效GLP-1受体激动剂,具有降低体重和降血糖作用。本研究试图评价司美格鲁肽注射液对比二甲双胍在精神分裂症伴代谢综合征患者疗效与安全性研究 |
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Objectives of Study: |
Objective To conduct a study of Simeglutide versus metformin for the treatment of schizophrenia with metabolic syndrome. Both mental illness itself and antipsychotic medications increase the risk of metabolic syndrome and diabetes, and previous studies have demonstrated that metformin has the ability to reduce antipsychotic-induced weight gain reported, but metformin use requires regular daily dosing, which poses a significant challenge for patients with poor adherence to psychiatric disorders. Simeglutide injection, a once-weekly long-acting GLP-1 receptor agonist, is known to have weight reduction and hypoglycaemic effects. This study sought to evaluate the efficacy and safety study of Simeglutide injection compared to metformin in patients with schizophrenia with metabolic syndrome |
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药物成份或治疗方案详述: |
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Description for medicine or protocol of treatment in detail: |
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纳入标准: |
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Inclusion criteria |
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排除标准: |
1.有Ⅰ型糖尿病史; 2.筛选时患有T2D的受试者:未经控制和潜在不稳定的糖尿病眼底病变,糖尿病肾病; 3.筛选时存在肾功能损害,血肌酐>150μmol/L或eGFR<45ml/(min·1.73m2),肝功能损害(转氨酶指标大于检验范围上限2倍),胰腺功能损害患者,严重心脏功能患者,难以控制高血压(收缩压>180mmhg或舒张压>100mmhg)。 4.最近90天内服用过减肥药。 5.存在使用司美格鲁肽注射液和二甲双胍任何禁忌症情况; 6.接受皮质类固醇或其他激素治疗(雌激素除外)的患者; 7.筛选时处于急性精神病期间(CGI-S评分≥6分)和有自杀行为; 8.计划或正在妊娠或哺乳患者; 9.物质滥用患者。 |
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Exclusion criteria: |
1. Have a history of type I diabetes; 2. Subjects with T2D at screening: uncontrolled and potentially unstable diabetic fundus lesions, diabetic nephropathy; 3. Patients with renal impairment at screening, serum creatinine > 150 μmol/L or eGFR < 45ml/(min·1.73m2), liver function impairment (aminotransferase index greater than 2 times the upper limit of the test range), patients with pancreatic function impairment, patients with severe cardiac function, difficulty in controlling hypertension (systolic blood pressure> 180mmHg or diastolic blood pressure >100mmhg). 4. Have taken weight loss medications within the last 90 days. 5. There are any contraindications to the use of semaglutide injection and metformin; 6. Patients receiving corticosteroids or other hormonal therapy (except estrogen); 7. Be in the acute mental illness (CGI-S score ≥ 6) and have suicidal behavior at the time of screening; 8. Patients who plan to be pregnant or breastfeeding; 9. Substance abuse patients. |
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研究实施时间: Study execute time: |
从 From 2024-01-15 00:00:00至 To 2026-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2025-01-07 00:00:00 至 To 2026-12-31 00:00:00 |
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干预措施: Interventions: |
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研究实施地点: Countries of recruitment and research settings: |
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测量指标: Outcomes: |
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采集人体标本:
Collecting sample(s)
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征募研究对象情况: Recruiting status: |
尚未开始 Not yet recruiting |
年龄范围: Participant age: |
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性别: |
男女均可 |
Gender: |
Both |
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随机方法(请说明由何人用什么方法产生随机序列): |
由社工采用随机数字表法实施分配 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Social workers use the random number table method to implement the distribution |
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是否公开试验完成后的统计结果: Calculated Results after the Study Completed public access: |
不公开/Private |
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盲法: |
开放标签 |
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Blinding: |
Open-label study |
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是否共享原始数据: IPD sharing |
否No |
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共享原始数据的方式(说明:请填入公开原始数据日期和方式,如采用网络平台,需填该网络平台名称和网址): |
无 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
None |
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数据采集和管理(说明:数据采集和管理由两部分组成,一为病例记录表(Case Record Form, CRF),二为电子采集和管理系统(Electronic Data Capture, EDC),如ResMan即为一种基于互联网的EDC: |
病例记录表 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
CRF |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
无/No |