Effect of Remote Ischemic Preconditioning on Lung Injury After Pulmonary Resection
NCT ID: NCT01307085
Last Updated: 2013-12-12
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
108 participants
INTERVENTIONAL
2011-02-28
2013-06-30
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
DOUBLE
Study Groups
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preconditioning
Adult patients undergoing elective pulmonary lobectomy were received a remote ischemic preconditioning group after induction of anaesthesia.
remote ischemic preconditioning
Remote ischaemic preconditioning consisted of three 5-min cycles of right upper limb ischaemia, induced by an automated cuff-inflator placed on the upper arm and inflated to 200 mm Hg, with an intervening 5 min of reperfusion during which the cuff was deflated.
conventional
Adult patients undergoing pulmonary lobectomy were received no treatment after induction of anaesthesia.
No interventions assigned to this group
Interventions
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remote ischemic preconditioning
Remote ischaemic preconditioning consisted of three 5-min cycles of right upper limb ischaemia, induced by an automated cuff-inflator placed on the upper arm and inflated to 200 mm Hg, with an intervening 5 min of reperfusion during which the cuff was deflated.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Must be received pulmonary lobectomy
Exclusion Criteria
* Preoperative severe impairment of respiratory function (arterial oxygen tension (PaO2) \<60 mmHg or FEV1\<50% predicted),
* Pre-existing coagulopathy or thrombocytopenia
* Prior receipt of chemotherapy or radiation therapy or immunotherapy
* Systemic or local active infections (either clinically defined or suggested by evidence such as elevated C-reactive protein levels, leukocytosis, or a body temperature\>38℃)
* Peripheral vascular disease affecting the upper limbs
* Administration of vitamins, nonsteroidal anti-inflammatory agent or corticosteroid within 3 months.
18 Years
65 Years
ALL
No
Sponsors
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Cai Li
OTHER
Responsible Party
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Cai Li
Department of Anesthesiology, First Affiliated Hospital, Sun Yat-Sen University
Principal Investigators
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Xuan Ke Liu, Ph.d
Role: PRINCIPAL_INVESTIGATOR
Department of Anesthesiology, The First Affiliated Hospital, Sun Yat-sen University
Locations
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Departmeng of Anesthesiology, The First Affiliated Hospital, Sun Yat-sen University
Guangzhou, Guangdong, China
Countries
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Other Identifiers
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RIP1126
Identifier Type: -
Identifier Source: org_study_id