ISRCTN50581876已完成未知
Resolution of Organ Injury in Acute Pancreatitis (RESORP): an observational cohort study with a nested cohort
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 229
研究概览
简要总结
2020 Protocol article in https://pubmed.ncbi.nlm.nih.gov/33293311/ (added 10/03/2022)
研究设计
- 研究类型
- Observational
入排标准
- 性别
- All
入选标准
- •1. All patients treated at Royal Infirmary Edinburgh with a clinical or radiological diagnosis of acute pancreatitis will be recruited where possible
- •2. For the potential clinical diagnosis of acute pancreatitis an appropriate clinical history based on compatible clinical features, will be required (i.e. abdominal pain, nausea and/or vomiting), supported by the finding of elevated serum amylase greater than 3x the upper limit of the reference range for the laboratory (currently 300 U/L)
- •3. For the radiological diagnosis, if applicable, computerised tomography (CT) and/or ultrasound scan (USS) evidence of acute pancreatitis will be accepted
- •4. With the exception of prisoners, all adult patients with capacity to give informed consent will be considered
排除标准
- •Current exclusion criteria as of 09/04/2024:
- •1. Patients under the age of 16 years will be excluded from the present study
- •2. Prisoners will be excluded from the present study
- •3. Patients lacking the capacity to consent will be excluded but can be included if they regain capacity during the hospital admission
- •The additional two exclusions below apply only to those patients being considered for the nested cohort study:
- •4. Patients not able to undergo MRI scanning for technical reasons will be excluded (e.g. those with cochlear implants, implanted pacemaker)
- •5. Patients with a known allergy to salbutamol
- •Previous Participant exclusion criteria (as of 18/12/2017):
- •1. Patients under the age of 16 years will be excluded from the present study
- •2. Prisoners will be excluded from the present study
- •3. Patients lacking the capacity to consent will be excluded but can be included if they regain capacity
- •The additional two exclusions below apply only to those patients being considered for the nested cohort study:
- •4. Patients not able to undergo MRI scanning for technical reasons will be excluded (e.g. those with cochlear implants, implanted pacemaker)
- •5. Patients with a known allergy to salbutamol
- •Previous Participant exclusion criteria:
- •1. Patients under the age of 16 years will be excluded from the present study
- •2. Prisoners will be excluded from the present study
- •3. Patients lacking the capacity to consent will be excluded but can be included if they regain capacity
- •4. Patients not able to undergo MRI scanning for technical reasons will be excluded (e.g. those with cochlear implants, implanted pacemaker)
- •5. An additional exclusion will apply only to those patients being considered for the nested cohort study: patients with a known allergy to salbutamol
研究者
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