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Clinical Trials/ChiCTR2100050281
ChiCTR2100050281Not yet recruitingNot Applicable

利那洛肽联合复方聚乙二醇电解质散在老年患者结肠镜检查前肠道准备效果的研究

重庆市科委1 site in 1 country333 target enrollmentStarted: September 1, 2021Last updated:
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
333
Locations
1
Primary Endpoint
肠道准备质量的评估

Study Overview

Brief Summary

提高老年患者在结肠镜检查前的肠道准备效果。

Study Design

Study Type
干预性研究
Primary Purpose
随机平行对照
Masking
None

Eligibility Criteria

Ages
60 to — (—)
Sex
All

Inclusion Criteria

  • 1.年龄>=60 岁者;男女不限;
  • 2.按计划做结肠镜检查者。

Exclusion Criteria

  • 1.严重心力衰竭(心功能 III 或 IV 级);
  • 2.近期急性心肌埂塞或不稳定性心绞痛;
  • 4.疑似肠梗阻或穿孔;
  • 8.有精神疾病不能配合检查者;
  • 9.对肠道准备药物不耐受或过敏者。

Arms & Interventions

A 组

利那洛肽联合 2L PEG 组

C 组

2L PEG

B 组

3L PEG

Intervention: 3L PEG

Outcomes

Primary Outcomes

肠道准备质量的评估

Secondary Outcomes

  • 肠道准备过程中的不良反应及接受度
  • 结肠镜检情况
  • 经济效益分析

Investigators

Sponsor
重庆市科委

Study Sites (1)

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