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注册号: Registration number: |
ChiCTR2100047386 |
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最近更新日期: Date of Last Refreshed on: |
2022-02-07 11:47:13 |
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注册时间: Date of Registration: |
2021-06-13 00:00:00 |
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注册号状态: |
补注册 |
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Registration Status: |
Retrospective registration |
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注册题目: |
Outcomes of OAGB/MGB as Conversional Surgery after Failed Sleeve Gastrectomy |
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Public title: |
Outcomes of OAGB/MGB as Conversional Surgery after Failed Sleeve Gastrectomy |
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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: |
Mid-term Outcomes of OAGB/MGB as Conversional Surgery after Failed Sleeve Gastrectomy; A Tertiary Center Experience |
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Scientific title: |
Mid-term Outcomes of OAGB/MGB as Conversional Surgery after Failed Sleeve Gastrectomy; A Tertiary Center Experience |
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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: |
Mohammad Kermansaravi |
研究负责人: |
Mohammad Kermansaravi |
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Applicant: |
Mohammad Kermansaravi |
Study leader: |
Mohammad Kermansaravi |
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申请注册联系人电话: Applicant telephone: |
+98 91 28874084 |
研究负责人电话:
Study leader's |
+98 91 28874084 |
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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: |
kermansaravi.m@iums.ac.ir |
研究负责人电子邮件: Study leader's E-mail: |
kermansaravi.m@iums.ac.ir |
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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: |
Hazrat e Rasool Hospital, Shahid Mansouri Ave, Niyayesh StSattarkhan St, Setayesh Street, No 98, Tehran, Iran |
研究负责人通讯地址: |
Hazrat e Rasool Hospital, Shahid Mansouri Ave, Niyayesh StSattarkhan St, Setayesh Street, No 98, Tehran, Iran |
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Applicant address: |
Hazrat e Rasool Hospital, Shahid Mansouri Ave, Niyayesh StSattarkhan St, Setayesh Street, No 98, Tehran, Iran. |
Study leader's address: |
Hazrat e Rasool Hospital, Shahid Mansouri Ave, Niyayesh StSattarkhan St, Setayesh Street, No 98, Tehran, Iran. |
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申请注册联系人邮政编码: Applicant postcode: |
1449614535 |
研究负责人邮政编码: Study leader's postcode: |
1449614535 |
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申请人所在单位: |
伊朗德黑兰Rasoole Akram Hospital |
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Applicant's institution: |
Minimally Invasive Surgery Research Center, Division of Minimally Invasive and Bariatric Surgery, Department of Surgery, Rasoole Akram Hospital, Iran University of Medical Sciences, Tehran, Iran |
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研究负责人所在单位: |
伊朗德黑兰Rasoole Akram Hospital |
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Affiliation of the Leader: |
Minimally Invasive Surgery Research Center, Division of Minimally Invasive and Bariatric Surgery, Department of Surgery, Rasoole Akram Hospital, Iran University of Medical Sciences, Tehran, Iran |
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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: |
IR.IUMS.REC.1399.801 |
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: |
Iran University of Medical Sciences (Ethics Committee in Biomedical Research) |
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Name of the ethic committee: |
Iran University of Medical Sciences (Ethics Committee in Biomedical Research) |
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伦理委员会批准日期: Date of approved by ethic committee: |
2020-11-11 00:00:00 | ||
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伦理委员会联系人: |
Iran University of Medical Sciences (Ethics Committee in Biomedical Research) |
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Contact Name of the ethic committee: |
Iran University of Medical Sciences (Ethics Committee in Biomedical Research) |
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伦理委员会联系地址: |
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Contact Address of the ethic committee: |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
ethics@behdasht.gov.ir | |
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研究实施负责(组长)单位: |
Iran University of Medical Sciences |
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Primary sponsor: |
Iran University of Medical Sciences |
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研究实施负责(组长)单位地址: |
Hazrat e Rasool Hospital, Shahid Mansouri Ave, Niyayesh StSattarkhan St, Setayesh Street, No 98, Tehran, Iran. |
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Primary sponsor's address: |
Hazrat e Rasool Hospital, Shahid Mansouri Ave, Niyayesh StSattarkhan St, Setayesh Street, No 98, Tehran, Iran. |
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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: |
Vice Chancellor for Research & Technology, Iran university of medical sciences |
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Source(s) of funding: |
Vice Chancellor for Research & Technology, Iran university of medical sciences |
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研究疾病: |
morbid obesity |
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Target disease: |
morbid obesity |
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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: |
回顾性研究 | ||||||||||||||||||||||
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Study phase: |
Retrospective study |
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研究设计: |
横断面 |
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Study design: |
Cross-sectional |
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研究目的: |
General objectives: 1. Determining weight changes and comorbidities after OAGB/MGB Sub-objectives: 1. Determining the amount of BMI changes after OAGB/MGB 2. Determining the extent of EWL changes after OAGB/MGB 3. Determining the changes in diabetes after OAGB/MGB 4. Determination of changes in blood pressure after OAGB/MGB in patients with hypertension Determining the changes of obstructive sleep apnea after OAGB/MGB in patients with obstructive sleep apnea Determination of GERD changes after OAGB/MGB in patients with GERD 7. Determination of dyslipidemia changes after OAGB/MGB patients with dyslipidemia 8. Determining the indications for conversion 9. Determination of surgical complications following OAGB/MGB 10. Determining patients' demographic information |
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Objectives of Study: |
General objectives: 1. Determining weight changes and comorbidities after OAGB/MGB Sub-objectives: 1. Determining the amount of BMI changes after OAGB/MGB 2. Determining the extent of EWL changes after OAGB/MGB 3. Determining the changes in diabetes after OAGB/MGB 4. Determination of changes in blood pressure after OAGB/MGB in patients with hypertension Determining the changes of obstructive sleep apnea after OAGB/MGB in patients with obstructive sleep apnea Determination of GERD changes after OAGB/MGB in patients with GERD 7. Determination of dyslipidemia changes after OAGB/MGB patients with dyslipidemia 8. Determining the indications for conversion 9. Determination of surgical complications following OAGB/MGB 10. Determining patients' demographic information |
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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: |
Patients whose indication for surgery is early complications (less than 8 weeks) after surgery, such as a stapler line leak. |
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Exclusion criteria: |
Patients whose indication for surgery is early complications (less than 8 weeks) after surgery, such as a stapler line leak. |
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研究实施时间: Study execute time: |
从 From 2016-01-01 00:00:00至 To 2020-09-01 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2016-01-02 00:00:00 至 To 2020-08-31 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: |
结束 /Completed |
年龄范围: Participant age: |
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性别: |
男性 |
Gender: |
Male |
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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): |
No |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
not applicable due to being retrospective |
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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: |
公开/Public |
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盲法: |
N/A |
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Blinding: |
not applicable |
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试验完成后的统计结果(上传文件): |
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Calculated Results after
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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): |
Not stated |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Not stated |
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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: |
Based on national obesity surgery database, the data will be collected at the time of SG and OAGB/MGB including age, gender, weight, height, nadir weight, BMI, percent excess weight loss (%EWL): %EWL=[(Initial Weight) – (Post-Op Weight)]/[(Initial Weight) – (Ideal Weight)] [7] and conversion indication. Some obesity-related comorbidities including type-2 Diabetes Mellitus (DM), arterial Hypertension (HTN), dyslipidemia, Obstructive Sleep Apnea (OSA) and GERD. Weight indicators and comorbidity outcomes are evaluated 1, 2, 3 and 5 years after the conversion surgery. The changes in comorbidities are classified in five categories: No change, remission, improvement, new onset and recurrence, which are assessed according to standardized outcomes reporting in metabolic and bariatric surgery. |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Based on national obesity surgery database, the data will be collected at the time of SG and OAGB/MGB including age, gender, weight, height, nadir weight, BMI, percent excess weight loss (%EWL): %EWL=[(Initial Weight) – (Post-Op Weight)]/[(Initial Weight) – (Ideal Weight)] [7] and conversion indication. Some obesity-related comorbidities including type-2 Diabetes Mellitus (DM), arterial Hypertension (HTN), dyslipidemia, Obstructive Sleep Apnea (OSA) and GERD. Weight indicators and comorbidity outcomes are evaluated 1, 2, 3 and 5 years after the conversion surgery. The changes in comorbidities are classified in five categories: No change, remission, improvement, new onset and recurrence, which are assessed according to standardized outcomes reporting in metabolic and bariatric surgery. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |