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Clinical Trials/ChiCTR2200066122
ChiCTR2200066122Not yet recruitingUnknown

一种胸腔镜手术相关成人慢性术后疼痛预测模型的开发与验证:一项前瞻性队列研究

Not provided1 site in 1 country500 target enrollmentStarted: December 1, 2022Last updated:

Trial Snapshot

Phase
Unknown
Status
Not yet recruiting
Enrollment
500
Locations
1
Primary Endpoint
术后三个月慢性疼痛发生率

Study Overview

Brief Summary

开发并验证一种胸腔镜手术相关成人慢性术后疼痛预测模型,指导早期识别可能发生胸腔镜相关 CPSP 的患者

Study Design

Study Type
Observational

Eligibility Criteria

Ages
18 to — (—)
Sex
All

Inclusion Criteria

  • (1)年龄≥18 岁,性别不限;
  • (2)美国麻醉医师分级(ASA)I~Ⅲ级;
  • (3)计划在全身麻醉下行胸腔镜肺部手术;
  • (4)清楚了解研究过程并自愿参加本研究,签署知情同意书。

Exclusion Criteria

  • (3)未行胸腔镜手术或术中改变术式;
  • (5)既往行胸外科手术患者;
  • (6)初次手术后 3 个月内需要再次手术,则回顾性排除患者;
  • (7)术前存在认知障碍或无法进行有效的沟通交流。

Arms & Interventions

1 组

Outcomes

Primary Outcomes

术后三个月慢性疼痛发生率

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Not provided

Study Sites (1)

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