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Injection of local anaesthetic with or without adjuvant in neck under sonography guidance in order to anaesthetise forearm and hand

Comparison of plain Ropivacaine versus Ropivacaine with different concentration of Dexmedetomidine in ultrasound guided supraclavicular block for Orthopedic forearm surgery-A prospective , randomised , comparative clinical study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/11/010327
Enrollment
75
Registered
2017-11-01
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- Upper limb fractures

Interventions

Intervention1: Supraclavicular brachial plexus block: Supraclavicular block with 1.plain ropivacaine vs 2.plain ropivacaine with 50mic dexmedetomidine vs 3.plain ropivacaine with 100mic dexmedetomid

Sponsors

Parul sevashram hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.ASA grade 1 and 2 2.Both elective and emergengy surgeries. 3.Upper limb surgeries-elbow,forearm and hand 4.Patient able to give informed and written consent

Exclusion criteria

Exclusion criteria: 1.Allergy or hypersensitivity to local anaesthtic agent 2. Patient with bleeding disorder or on anticoagulant therapy 3. Pregnant patient 4. Patient with major cardiovascular,respiratory ,renal,and liver disease 5. Patient taking opiod medicine

Design outcomes

Primary

MeasureTime frame
1. Duration of analgesia 2. Duration of sensory and motor blockTimepoint: 1. From end of surgery to pain on VAS OF 4 or more.. 2. From onset of block to start of recovery

Secondary

MeasureTime frame
Adverse effects, sedation score, rescue analgesicTimepoint: Every 2 hourly upto 24 hrs

Countries

India

Contacts

Public ContactDr Amit P Chauhan

PARUL INSTITUTE OF MEDICAL SCIENCE AND RESEARCH

dramitchauhan8885@gmail.com9426368170

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026