University of Texas MD Anderson Cancer Center
Houston, Texas, 77030, United States
NCT Number: NCT01692210
The goal of this research study is to learn about how dexmedetomidine (a standard of care sedative) affects your immune system (your defenses against cancer) by measuring your white blood cell levels before and after surgery.
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Notify Me18 year and older
Female
Observational
Houston, Texas, 77030, United States
Dexmedetomidine is a type of sedative used as part of anesthetic care. It is sometimes used to help lower the amount of pain killers and other anesthetics that are given to a patient during surgery. Researchers want to study how this drug works in cancer patients and review the patient's chart for pain levels and medication use after surgery. Part of this research involves studying the immune system of surgery patients.
If you agree to take part in this study, blood (about 1 tablespoon) will be drawn before you have surgery and the morning after surgery while you are still in the hospital. This blood will be used to learn more about how your immune system works.
After your second blood draw, your participation in this study will be over.
This is an investigational study.
Up to 20 participants will be enrolled in this study. All will take part at MD Anderson.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
3.1.1 - Women undergoing unilateral mastectomy for malignancy at MD Anderson Cancer Center.
3.1.2 - Patients 18 years of age and older. There will be no upper age restriction.
3.1.3 - Patients must sign a study-specific consent form.
Exclusion criteria
3.2.1 - ASA 4
3.2.2 - Contraindication to the use of dexmedetomidine.
3.2.2.1. Decompensated congestive heart failure.
3.2.2.2. Second and third degree heart block.
3.2.2.2. Known allergy to dexmedetomidine or any of the medications used in the study
3.2.3 - Patients taking clonidine for treatment of arterial hypertension.
3.2.4 - Patients that are pregnant.
3.2.5 - Patients taking opioids at the time of surgery.
3.2.6 - Patients having plastic surgical reconstruction.
3.2.7 - Recent chemotherapy (< 4 weeks).
3.2.8 - Active autoimmune or immunological disease including but not limited to systemic lupus erythematous, rheumatoid arthritis and Sjogren's disease
3.2.9 - Patient refusal to participate in the study.
After induction of general anesthesia, a loading dose of dexmedetomidine (1 mcg/kg) given in 15 min followed by an infusion of the same medication at a rate of 0.4 - 0.7 mcg/kg/hour.
Time frame: 2 days
Lymphocyte counts determined by flow-cytometry and their function by cytotoxicity assays performed in the laboratory using samples obtained before and the morning after surgery. Patients who experience a reduction of less than 50% of their preoperative natural killer cell (NKC) activity considered as a success.
M.D. Anderson Cancer Center
Other
The Effect of Dexmedetomidine on Immunological Parameters of Women Undergoing Breast Cancer Surgery
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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