Aortic Valve Disorder Clinical Trial
Official title:
Comparison of Periosteal and Subcutaneous Infusions of Articaine and Bupivacaine in Treatment of Acute Pain After Sternotomy
Verified date | May 2019 |
Source | Helsinki University Central Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to examine the wound infusion of articaine for treatment of acute post-sternotomy pain in a placebo-controlled manner using a prospective and randomized design and an active control (bupivacaine)
Status | Suspended |
Enrollment | 36 |
Est. completion date | December 2022 |
Est. primary completion date | December 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility |
Inclusion Criteria: - elective procedure - open heart surgery - aortic valve surgery - mitral valve surgery - atrial septal defect repair surgery - intracardial myxoma removal surgery Exclusion Criteria: - local anesthetic allergy - sulphide allergy - asthma - pregnant women - neurological disease (TIA excluded) - congestive heart failure - left ventricle ejection fracture under 0.3 - liver failure - diabetes mellitus with documented polyneuropathy - chronic pain condition - mother tongue not finnish or swedish - patients, who do not agree blood transfusions |
Country | Name | City | State |
---|---|---|---|
Finland | Department of Anesthesiology and Intensive care medicine, Divison of Surgery, Meilahti hospital, Helsinki University Central Hospital | Helsinki | Uusimaa |
Finland | Department of Cardiothoracic surgery, Division of Surgery, Meilahti hospital, Helsinki University Central Hospital | Helsinki | Uusimaa |
Lead Sponsor | Collaborator |
---|---|
Helsinki University Central Hospital |
Finland,
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* Note: There are 20 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Oxycodone consumption | 72 hours from initiation of treatment | ||
Secondary | Intensity of pain in rest/in movement (AUC) | 72 hours from initiation of treatment |
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