New York, New York 10021

  • Pain Management Following Cardiopulmonary Bypass Surgery

Purpose:

This study evaluates the safety and efficacy of ketorolac for post-operative pain management after heart surgery. Ketorolac appears to provide enhanced pain relief while also decreasing the requirements for morphine during the (immediate) 24-hour post-operative period.


Study summary:

Current practice at this institution does not include routine use of ketorolac for post-operative pain management of patients undergoing cardiac surgery. The investigators hypothesize that using Ketorolac as an adjunct to IV morphine can positively impact patient outcomes and reduce the occurrence of possible side effects.


Criteria:

Inclusion Criteria: - Males and females > 18 years of age at the screening visit. - Undergoing coronary artery bypass graft or single valve repair or replacement requiring cardiopulmonary bypass. - American Society of Anesthesiology (ASA) Physical Class 3, or 4. - Willing able to use a PCA Pump - Willing to receive iv morphine for 24 hours post initial ketorolac dose to control pain. - Capable of speaking and understanding English sufficiently to provide written informed consent and responses to pain assessment scales and neurological questionnaires. Exclusion Criteria: - Allergy or sensitivity to nonsteroidal anti-inflammatory drugs - History of gastrointestinal bleeding or peptic ulcer - Serum creatinine = 2.0 mg/dl or rise in serum creatinine of = 0.5 mg/dl or 25% within the preceding 10 days if known with the exception of patients with Dialysis Dependent End Stage Renal Disease (ESRD). - Hepatic dysfunction - Patients with low cardiac output syndrome (cardiac index < 2.0) after cardiopulmonary bypass or pre-op ejection fraction < 30% - Inability to operate PCA pump - Cardiothoracic reoperations - Bleeding disorder


NCT ID:

NCT00161577


Primary Contact:

Principal Investigator
Gergory Kerr, M.D., MBA
Weill Medical College of Cornell University, New York Presbyterian Hospital


Backup Contact:

N/A


Location Contact:

New York, New York 10021
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: April 03, 2020

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