RecruitingNot ApplicableNCT06910644

Dexmedetomidine Versus Lidocaine Infusions as Adjuvants to General Anesthesia for Chronic Pain Management After Mastectomy

Dexmedetomidine Versus Lidocaine Infusions as Adjuvants to General Anesthesia for Chronic Pain Management After Mastectomy: A Randomized Controlled Trial


Sponsor

Cairo University

Enrollment

90 participants

Start Date

Apr 5, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

This study aims to compare dexmedetomidine and lidocaine infusions as adjuvants to general anesthesia for chronic pain management after mastectomy.


Eligibility

Sex: FEMALEMin Age: 18 YearsMax Age: 75 Years

Inclusion Criteria3

  • Age from 18 to 75 years.
  • American Society of Anesthesiologists (ASA) physical status II.
  • Scheduled for mastectomy with axillary dissection (either modified radical mastectomy with or without latissimus dorsi flap or conservative breast surgery) due to breast cancer.

Exclusion Criteria6

  • Patient refusal.
  • Known allergy to any of the study drugs.
  • Those with hepatic or renal insufficiency.
  • Patients who are running regularly on B blockers.
  • α2 adrenergic agonists and sedatives.
  • Psychoactive medications.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGDexmedetomidine

Patients will receive 1 μg/kg of intravenous dexmedetomidine over 10 min followed by an intravenous infusion of 0.5 μg/kg/h.

DRUGLidocaine

Patients will receive a bolus of intravenous lidocaine 1.5mg/kg over 10 min followed by a continuous infusion of lidocaine 1.5mg/kg/h.

DRUGIsotonic saline

Patients will receive intravenous isotonic saline 0.9% in the same volume and manner as the study drugs.


Locations(1)

Cairo University

Cairo, Egypt

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06910644


Related Trials