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Comparison of duration of analgesic efficacy of Ropivacain given perineurally alone and mixed with dexamethasone and dexamethasone given intravenous in USG guided supraclavicular brachial plexus block.

Analgesic efficacy of Ropivacaine when injected perineural alone,mixed with dexamethasone and when dexamethasone given separately intravenous in USG guided supraclavicular brachial plexus block:A quasi experimental study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2019/04/018591
Enrollment
105
Registered
2019-04-15
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: M843- Stress fracture

Interventions

Control Intervention1: Group-RC: Ultra sonography guided supraclavicular brachial plexus block given with .5 percent ropivacaine 28ml plus normal saline 2ml and normal saline 5ml intravenous Control I

Sponsors

Department Of Anaesthesiology and Critical Care
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Body weight 30 to 80 kilograms 2.Patients belonging to ASA 1 and 2 3.Patients undergoing upper limb orthopedic surgeries of less than 3 hours duration 4.All laboratory investigations within normal limits 5.Patients free from any associated acute or chronic systemic illnesses

Exclusion criteria

Exclusion criteria: 1.Uncooperative patients 2.Patients hypersensitive to drugs ropivacaine and dexamethasone 3.Local pathology or deformities at site of block 4.Patients with ASA grade 3 and 4 5.Pregnant with lactating mother diabeic neurological deficiet 6.Patients with chronic pain on analgesics

Design outcomes

Primary

MeasureTime frame
Time of first rescue analgesic (Duration of analgesia):- min Number of times rescue analgesic given in 24 hrs:-1, 2, 3, 4, 5. Total dose of tramadol consumption in 24 hrs: mg Total dose of diclofenac consumption in 24 hrs: mg Timepoint: Time Before block 0 Hour (Just after block) 2 Hour 4 Hour 6 Hour 8 Hour 10 Hour 12 Hour 14 Hour 16 Hour 18 Hour 20 Hour 22 Hour 24 Hour—

Secondary

MeasureTime frame
1. To compare post-operative rescue analgesic (tramadol) consumption in first 24 hours. 2. NRS pain scores at rest(NRS-R)& at movement(passive/active)NRS-M of operated upper limb in first 24 hours. 3. Any changes in NIBP,PR.SpO2in first 24 hours 4. Patientâ??s satisfaction score. 5. Any complications / adverse effects/side effects of block. Timepoint: Time Before block 0 Hour (Just after block) 2 Hour 4 Hour 6 Hour 8 Hour 10 Hour 12 Hour 14 Hour 16 Hour 18 Hour 20 Hour 22 Hour 24 Hour—

Countries

India

Contacts

Public ContactDrDARAGA RAM CHOUDHARY

S.N.Medical College Jodhpur

dr.rakeshkarnawat@yahoo.com9828033321

Outcome results

None listed

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