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Clinical Trials/ChiCTR-IPR-17013365
ChiCTR-IPR-17013365Not yet recruitingPhase 4

肥胖患者围术期精准药物治疗的方案比较

自筹1 site in 1 country200 target enrollmentStarted: December 1, 2017Last updated:

Trial Snapshot

Phase
Phase 4
Status
Not yet recruiting
Sponsor
Enrollment
200
Locations
1
Primary Endpoint
奥美拉唑的血药浓度

Study Overview

Brief Summary

本研究旨在揭示质子泵抑制剂(以奥美拉唑注射剂为代表)的不同给药方式对围术期肥胖症患者的药代动力学改变,以及临床疗效的对比观察,为此类患者提供安全有效的用药推荐。

Study Design

Study Type
干预性研究
Primary Purpose
随机平行对照

Eligibility Criteria

Ages
18 to 50 (—)
Sex
All

Inclusion Criteria

  • ① 接受袖状胃切除术或胃转流术术后的肥胖症患者(BMI≥26kg/m2)

Exclusion Criteria

  • 有长期质子泵抑制剂用药史的患者

Arms & Interventions

A

奥美拉唑持续静脉推注

B

奥美拉唑静脉滴注

Outcomes

Primary Outcomes

奥美拉唑的血药浓度

Time Frame: 用药前(0h)以及用药后 24h

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
自筹

Study Sites (1)

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