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A clinical trial to study effect of Dexamethasone on duration of analgesia(pain relief) in brachial plexus block by Bupivacaine(local anaesthetic)

Phase 3
Conditions
Other specified injuries of elbowand forearm,
Registration Number
CTRI/2020/03/023757
Lead Sponsor
IAF
Brief Summary

Brachial plexus block is one of the preferred techniques for anaesthesia for upper limb surgeries. The advantage being that of analgesia lasting even after the anaesthesia with motor block wears off. Many adjuvants have been explored for co-administration along with the local anaesthetic to prolong this period. Each of these adjuvants has its own side effect profile, with this study we will attempt at understanding the analgesic effect and duration and also the side effect profile by comparing blood sugar levels and duration of motor blockade.

Detailed Description

Not available

Recruitment & Eligibility

Status
Other
Sex
All
Target Recruitment
32
Inclusion Criteria
  • Posted for Open Reduction Internal Fixation of UpperLimb fractures 2.
  • Upper limb surgery where Supraclavicular brachial plexus block is indicated.
Exclusion Criteria
  • Weight less than 40 Kg 2.
  • Pregnancy 3.
  • Poor sensorium (GCS < 13) 4.
  • Contraindications to Dexamethasone 5.
  • Diabetes Mellitus 6.
  • Patients on current steroid therapy or within past 6 weeks.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Compare the duration of Analgesia of brachial plexus block and time to first additional analgesicMeasured over 48 hours
Secondary Outcome Measures
NameTimeMethod
Duration of motor weakness of arm measured every 6 hoursMeasured over 48 hours
Postoperative blood sugar every 6 hoursMeasured over 48 hours

Trial Locations

Locations (1)

Air Force Hospital

🇮🇳

Dehat, UTTAR PRADESH, India

Air Force Hospital
🇮🇳Dehat, UTTAR PRADESH, India
Aditya Sapra
Principal investigator
9680019684
adityasapra@gmail.com

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