The Clinic Study to Prevent Pulmonary Embolism in Patients With General Anesthesia Operation in Perioperative Period

Pulmonary Embolism Clinical Trial

Official title:

The Clinic Study to Prevent Pulmonary Embolism in Patients With General Anesthesia Operation in Perioperative Period

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02460952
• Other study ID #: 22704102
• Status: Recruiting
• Phase: N/A
• First received: June 1, 2015
• Last updated: June 2, 2015
• Start date: August 2014
• Est. completion date: August 2016

Study information

• Verified date: June 2015
• Source: Beijing Chao Yang Hospital
• Contact: n/a
• Is FDA regulated: No
• Health authority: China: Ministry of Health
• Study type: Observational

Clinical Trial Summary

The purpose of this study is to investigate the prevention of Pulmonary Embolism in Patients who With General Anesthesia Operation in Perioperative Period.

Description:

Patients who received general anesthesia operation in Beijing Chaoyang Hospital affiliated to Capital Medical University were collected. The incidence of pulmonary embolism in perioperative period and age, gender,the surgery , clinical stage, clinical efficacy assessment will be further analyzed.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 500
• Est. completion date: August 2016
• Est. primary completion date: January 2016
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 45 Years to 85 Years

Eligibility

Inclusion Criteria:

• The first time to accept the general anesthesia operation

Exclusion Criteria:

• Pregnancy.

• The function of liver and kidney disorder or serious abnormal electrolyte.

• The abnormal coagulation dysfunction and blood volume.

Study Design

Observational Model: Case Control, Time Perspective: Retrospective

Related Conditions & MeSH terms

• Embolism
• Pulmonary Embolism

Locations

Country	Name	City	State
China	Liu Sijie	Beijing	Beijing

Sponsors (1)

Lead Sponsor	Collaborator
Beijing Chao Yang Hospital

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The changes of patients'Lower extremity vein in perioperative period of general anesthesia operation		3 days before operation to 7 days after the operation	Yes