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INFRACLAVICULAR BLOCK USING DEXMED AND DEXAMETHASONE TO ROPIVACAINE

TO COMPARE THE ULTRASOUND GUIDED INFRACLAVICULAR BLOCK CHARACTERISTICS (ONSET & DURATION) USING DEXMEDETOMIDINE & DEXAMETHASONE AS ADJUVANTS TO ROPIVACAINE FOR UPPER LIMB SURGICAL INTERVENTIONS - NIL

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/12/060933
Enrollment
80
Registered
2023-12-29
Start date
Unknown
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Health Condition 1: M849- Disorder of continuity of bone, unspecified Health Condition 2: M20-M25- Other joint disorders

Interventions

Intervention1: Infraclavicular block using Local anesthetic under usg guidance: Comparing the effects( Onset and duration of sensory and motor blockage as well as analgesia )in ultrasound-guided Infra

Sponsors

Armed forces medical college, Pune
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.?ASA grade I, II, III, IV 2.?Age 18- 60years 3.?Patients listed for surgical intervention in upper limb 4.?Written informed consent of patient for the study

Exclusion criteria

Exclusion criteria: 1. Age 60 years 2. History of allergy to local anesthetic drugs being used in the block 3. Presence of any neurological deficit in the involved limb 4. Fractures involving clavicle, shoulder region and upper 1/3 rd of humerus 5. Local site infection 6. Any structural deformity of the injection site 7. History of coagulopathy or patients using anticoagulants 8. Peripheral vascular disease 9. Block which failed and converted to other Anaesthesia technique

Design outcomes

Primary

MeasureTime frame
Onset and duration of sensory and motor blockage as well as analgesia.Timepoint: Initially, every 3 min till full blockage is achieved then every 30 minutes for the first 2 hrs then every 2 hours in postop for 24 hrs.

Secondary

MeasureTime frame
Intraoperative monitoring of vitals (pulse rate, blood pressure, O2 saturation and adverse effect if any), duration of analgesia, complications (if any) along with supplemented analgesia Timepoint: every 15 min

Countries

India

Contacts

Public ContactDr Saurabh Sud

Armed forces medical college

Saurabhsood1975@gmail.com6005709381

Outcome results

None listed

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