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Clinical Trials/ChiCTR2000029326
ChiCTR2000029326RecruitingUnknown

超声引导下腹横肌阻滞联合腹直肌鞘阻滞对腹腔镜直肠癌手术患者的影响

Not provided1 site in 1 country78 target enrollmentStarted: January 22, 2020Last updated:
Conditions

Trial Snapshot

Phase
Unknown
Status
Recruiting
Enrollment
78
Locations
1
Primary Endpoint
舒芬太尼用量

Study Overview

Brief Summary

观察超声引导下 TAP 联合 RSB 对接受腹腔镜直肠癌手术患者术后疼痛强度的影响。

Study Design

Study Type
Interventional
Primary Purpose
随机平行对照
Masking
双盲

Eligibility Criteria

Ages
35 to 70 (—)
Sex
All

Inclusion Criteria

  • ASA I-III 级患者;
  • 能够理解和使用术后镇痛装置。

Exclusion Criteria

  • 需要联合其他器官切除(阑尾除外);
  • 术前肠梗阻需急诊手术。

Arms & Interventions

对照组

生理盐水

试验组 1

超声引导下腹横肌阻滞

试验组 2

超声引导下腹横肌阻滞联合腹直肌鞘阻滞

Outcomes

Primary Outcomes

舒芬太尼用量

Secondary Outcomes

  • 疼痛评分

Investigators

Sponsor
Not provided

Study Sites (1)

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