Actively Recruiting
Comparative Analysis Of Dexmedetomidine And Dexamethasone As An Adjuvant To 0.5%Ropivacaine On Onset Of Ultrasound Guided Supraclavicular Brachial Plexus Block In Patients Undergoing Upper Limb Surgeries
Led by Sahiwal medical college sahiwal · Updated on 2025-12-23
66
Participants Needed
1
Research Sites
60 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
To compare the efficacy of dexmedetomidine and dexamethasone as an adjuvant to 0.5%ropivacaine on onset of ultrasound guided supraclavicular brachial plexus block in patients undergoing upper limb surgeries. Ropivacaine hydrochloride, a long acting local anesthetic, is commonly used for supraclavicular block owing to its favorable safety profile especially in terms of minimal cardiotoxicity and less motor block. Dexmedetomidine, a highly selective alpha-2 adrenergic agonist, enhances the quality of supraclavicular block by providing sedation and analgesia while potentially prolonging the duration of block through hyperpolarization of nerve fibers. While, Dexamethasone, a synthetic corticosteroid with potent anti-inflammatory and immunosuppressive properties, prolongs duration of analgesia by reducing perineural inflammation and inhibiting nociceptive signal transmission. Supraclavicular brachial plexus block offers dense anesthesia for surgical procedures at or distal to the elbow with relatively high success rate, once described as "spinal of the arm". Moreover, supraclavicular brachial plexus block is an excellent alternative to general anesthesia in upper limb surgeries.
CONDITIONS
Official Title
Comparative Analysis Of Dexmedetomidine And Dexamethasone As An Adjuvant To 0.5%Ropivacaine On Onset Of Ultrasound Guided Supraclavicular Brachial Plexus Block In Patients Undergoing Upper Limb Surgeries
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients scheduled for upper limb surgery below mid-humerus level
- Patients aged 18 to 70 years
- Patients with ASA class I, II and III
- Male and non-pregnant females
You will not qualify if you...
- Patients refusal
- Patients with pre-existing peripheral neuropathy of the upper limb
- Patients with infection at block site
- Patients with history of ischemic heart disease
- Patients with bleeding disorder or deranged coagulation profile
- Patients with known history of allergy to local anesthetic or any other drugs used
AI-Screening
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Trial Site Locations
Total: 1 location
1
Sahiwal Medical College, Sahiwal
Sāhīwāl, Punjab Province, Pakistan, 57000
Actively Recruiting
Research Team
D
Dr Maryam Maqsood, MBBS
CONTACT
D
Dr Muhammad Shahid, FCPS
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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