跳至主要内容
临床试验/NCT04937335
NCT04937335已完成不适用

Clinical Features and Risk Factors of Craniopharyngioma With Tumoral Hemorrhage

Tongji Hospital0 个研究点目标入组 185 人开始时间: 2013年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
185
主要终点
craniopharyngioma with tumoral hemorrhage

研究概览

简要总结

Clinical data of 185 consecutive patients receiving resective operation with a pathological diagnosis of craniopharyngioma in our hospital between January 2013 and February 2021 were collected. Among these patients, 18 of them were recognized as craniopharyngioma with tumoral hemorrhage during the operation.

详细描述

For each case, age, gender, smoking status, alcohol intake, past history, symptoms, blood pressure, blood cell count, blood biochemical tests, coagulation tests, hormone tests, radiological results, surgical treatment and the outcome at discharge were collected. The first test result after admission and before the operation was taken for the items of blood tests with multiple times in the analysis.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Retrospective

入排标准

性别
All
接受健康志愿者

入选标准

  • receive resective operation with a pathological diagnosis of craniopharyngioma in our hospital
  • enter our hospital between January 2013 and February 2021

排除标准

  • have a non-craniopharyngioma or unverified pathological diagnosis at discharge
  • have received surgical or radiological treatment on the sellar region
  • receive treatment of coagulation modulation, immunosuppressive agents or chemotherapeutic drugs
  • combine with other clinical emergencies including acute myocardial infarction, cerebral stroke, trauma and sepsis at admission
  • have been diagnosed with other tumors, hematological diseases, autoimmune diseases, liver failure or renal failure

结局指标

主要结局

craniopharyngioma with tumoral hemorrhage

时间窗: during the operation

Current study is a case-control study whose primary outcome is tumoral hemorrhage observed during the operation, which devided the craniopharyngioma patients into hemorrhage group and non-hemorrhage group.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Kai Shu

Prof. Dr.

Tongji Hospital

相似试验