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Clinical Trials/ChiCTR2100048278
ChiCTR2100048278Not yet recruitingNot Applicable

探索不同节律类型人群术后疼痛情况的观察性研究

自选课题1 site in 1 country300 target enrollmentStarted: June 23, 2021Last updated:
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Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
300
Locations
1
Primary Endpoint
术后疼痛评估量表得分
Study OverviewStudy DesignEligibility CriteriaArms & InterventionsOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

探讨患者节律状态对术后疼痛的影响。

Study Design

Study Type
观察性研究
Primary Purpose
连续入组
Masking
N/a

Eligibility Criteria

Ages
18 to 70 (—)
Sex
All

Inclusion Criteria

  • •1.腹部外科手术的全麻患者；
  • •2.ASA 分级 I-III；
  • •3.愿意参加本研究并签署知情同意书。

Exclusion Criteria

  • •1.已知患有慢性疼痛的患者；
  • •2.术前长期服用镇痛药物或药物依赖患者；
  • •3.任何原因不能配合研究。

Arms & Interventions

连续入组

Outcomes

Primary Outcomes

术后疼痛评估量表得分

ME-Q 量表得分

Secondary Outcomes

  • 睡眠质量
  • 住院时间
  • 镇痛药消耗量

Investigators

Sponsor
自选课题

Study Sites (1)

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