Actively Recruiting

Phase 2
Phase 3
Age: 18Years - 70Years
All Genders
Healthy Volunteers
NCT07290595

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

Age: 18Years - 70Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

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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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