RecruitingNot ApplicableNCT06423859

Articaine Plus Dexmedetomidine in Supraclavicular Block

A Comparative Study Between Articaine Alone Versus Articaine Plus Dexmedetomidine for Ambulatory Orthopedic Surgery Under Supraclavicular Block


Sponsor

Benha University

Enrollment

66 participants

Start Date

Feb 1, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

Articaine has emerged as a local anesthetic (LA) that produces sensory and motor blockade shorter than bupivacaine and lower in neurotoxicity than lidocaine. Studies have shown that adding dexmedetomidine to LA produces prolongation of sensory and motor bock duration. Early regain of motor power with adequate analgesia is needed in ambulatory surgery, for early start of physiotherapy. This study was designed to test efficacy of adding dexmedetomidine to articaine on the duration of sensory and motor block.


Eligibility

Min Age: 18 YearsMax Age: 60 Years

Inclusion Criteria1

  • aged 18-60 years planned for upper limb surgery below the midhumerus with an expected time of less than 90 min usually under tourniquet.

Exclusion Criteria6

  • allergies to local anesthetic,
  • those with ASA III and IV,
  • patients who refuse to participate,
  • uncooperative patients,
  • patients who have infection at the site of injection,
  • patients who have bleeding disorder, and patients on anticoagulant drugs.

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Interventions

DRUGArticaine

supraclavicular brachial plexus block with articaine 2%

DRUGDexmedetomidine

supraclavicular brachial plexus block with articaine 2% in addition with Dexmedetomidine


Locations(1)

Samar Rafik Mohamed Amin

Banhā, Qalyubia Governorate, Egypt

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NCT06423859


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