Status:
TERMINATED
Analgesic Effect of Perioperative Systemic Lidocaine in Patients Undergoing Unilateral Mastectomy Surgery
Lead Sponsor:
Northwestern University
Conditions:
Pain
Eligibility:
FEMALE
18-65 years
Phase:
PHASE4
Brief Summary
The aim of this study is to determine if perioperative systemic lidocaine administration will decrease the amount of opioid analgesics required in women undergoing mastectomy surgery. In addition, pat...
Detailed Description
Patients will be recruited up to 21 days prior to the day of surgery. The consent form will be reviewed with the patient, and the patient will be allowed to take a copy home. If the patient does not h...
Eligibility Criteria
Inclusion
- Age: 18-65 years
- Gender: Female
- ASA Physical Status I-III
- Non-pregnant
- Surgery: Unilateral total or segmental mastectomy
- Language: English speaking
- Consent: Obtained
Exclusion
- Age: Under 18 or over 65 years
- ASA Physical Status \>III
- Pregnancy
- Language: Non-English speaking
- Allergy to Lidocaine or amide local anesthetics
- Contraindication to succinylcholine
- History and/or EKG evidence of conduction defect
- Renal failure (Creatinine \>1.7 mg/dL)
- Patient expected to remain intubated after procedure
- Chronic home opioid or steroid use
- Opioid use within one week prior to procedure
- Drug or alcohol abuse
- Inability to use PCA
Key Trial Info
Start Date :
May 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 1 2011
Estimated Enrollment :
22 Patients enrolled
Trial Details
Trial ID
NCT00913003
Start Date
May 1 2009
End Date
October 1 2011
Last Update
February 4 2015
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