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Effect of a drug on pain management given with regional block to reduce pain after surgery

comparative evaluation of ropivacaine and ropivacaine with dexmedetomidine in axillary brachial plexus block for post operative analgesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/05/025021
Enrollment
80
Registered
2020-05-05
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: S599- Unspecified injury of elbow and forearm

Interventions

Intervention1: ropivacaine 0.5% with dexmedetomidine for postoperative analgesia: ropivacaine 0.5% with dexmedetomidine for postoperative analgesia Control Intervention1: ropivacaine 0.5% with dexmede

Sponsors

Dr Ankita Rawat
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients with ASA grade I and II. 2.Age group 18- 60 years 3 Patient undergoing upper limb surgery under axillary block

Exclusion criteria

Exclusion criteria: 1.Patient refusal 2.ASA grade III & IV patients 3.History of allergy or sensitivity to local anaesthetic or study drug 4. Known cardiovascular respiratory disease 5.Known hepato renal disease 6.Neuropsychiatric disorders 7.History of bleeding disorder.. 8.Day care surgery 9.Pregnancy

Design outcomes

Primary

MeasureTime frame
To evaluate for the duration of post-operative analgesiaTimepoint: To evaluate for the duration of post-operative analgesia

Secondary

MeasureTime frame
1 .To evaluate the onset of sensory and motor block 2 To compare the complete effect of sensory and motor block 3. To assess for patient satisfaction 4. To evaluate the adverse effects like nausea, vomiting, dysarrhythmias, hypotension, bradycardia, convulsions, sedation, neurological problems and hypersensitivity reaction for the study drug . Timepoint: 1.from administration of drug upto the 30 minutes of surgery for sensory and motor block assessment 2.Visual analogue scoring for oain from the point completion of surgery upto 24 hrs

Countries

India

Contacts

Public ContactDr Urmila Palaria

GMC Haldwani

urmila_palaria@rediffmail.com9897088443

Outcome results

None listed

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