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NCT03938480 Clinical Trial

Duration Threstholds of Intraoperative Hypotension

Hypotension Clinical Trial

Official title:
Duration Threstholds of Intraoperative Hypotension for Postoperative Major Adverse Events

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03938480
Other study ID # DTIH
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2019
Est. completion date May 22, 2019

Study information
Verified date June 2019
Source Peking University First Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Intraoperative hypotension is common in non cardiac surgery. longer duration of intraoperative hypotension is related with postoperative morbidity and mortality. however, with the change of hypotension criteria, the duration threshold also change. the relationship of different hypotension criteria and its duration is unclear. This study is to explore the their relationship.

Description:

Intraoperative hypotension is common in non cardiac surgery. longer duration of intraoperative hypotension is related with postoperative morbidity and mortality. however, with the change of hypotension criteria, the duration threshold also change. the relationship of different hypotension criteria and its duration is unclear. This study is to explore the relationship between continous difference mean blood pressure criteria and its duration thresholds for postoperative major adverse events, which include acute cardiac infarction, heart failure, cardiac death, stroke and acute kidney injury.

Recruitment information / eligibility
Status Completed
Enrollment 37000
Est. completion date May 22, 2019
Est. primary completion date May 20, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria:

adults underwent elective non-cardiac surgery

Exclusion Criteria:

cardiac surgeries; kidney surgeries; obstetric surgeries; local infiltration anesthesia; surgeries without arterial pressure monitoring; perioperative data missing; patients with more than one operation within a year

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
China PKU 1st hospital Beijing Beijing

Sponsors (1)
Lead Sponsor Collaborator
Peking University First Hospital

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary major adverse events including acute cardiac infarction, heart failure, cardiac death, stroke, kidney injury 30 days postoperatively in hospital
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