To compare different doses of dexmedetomidine combined with ropivacaine to assess postoperative analgesia using ultrasound guided supraclavicular brachial plexus block in upper limb surgeries

A Randomized comparative study to Compare different doses of Dexmedetomidine combined with Ropivacaine to assess post-operative analgesia using ultrasound-guided Supraclavicular Brachial Plexus Block in Upper Limb Surgeries- in Department of Anaesthesia at SMS Hospital, Jaipur - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/03/064709

Enrollment

Registered

2024-03-22

Start date

Unknown

Completion date

Unknown

Last updated

2024-04-01

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

Conditions

Health Condition 1: V00-Y99- External causes of morbidity

Interventions

Intervention1: ultasound guided supraclavicular brachial plexus block in elective upper limb surgery: dexmedetomidine 25mcg combined with ropivacaine to assess postoperative duration of analgesia usi

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patient posted for upper limb surgeries 2. Either sex 3. Age-between 18 and 60 years 4. American Society ofAnesthesiologists Physical Status (ASA-PS) Classes I and II 5.Bodyweight: 40-70 kg 6.Patients who will give informed written consent

Exclusion criteria

Exclusion criteria: 1.Patient should not be a part of other study. 2.Nonco-operative patient. 3.Patients having severe systemic illness and bleeding disorders, 4.Pregnant women 5.Patients allergic to study drugs 6.Patients havingpre-existing sensory and motor deficit 7.Local site infection or deformity if any at the injection site

Design outcomes

Primary

Measure	Time frame
1.Mean Duration of analgesia (minutes) 2.Mean of NRS score Timepoint: Postoperative 4hr Postoperative 8hr Postoperative 12hr Postoperative 16hr Postoperative 20hr Postoperative 24hr	—

Secondary

Measure	Time frame
1.Mean time of onset of sensory block (minutes) 2.Mean time of onset of motor block (minutes) 3.Mean Duration of motor block (minutes) 4.Median of sedation score 5.Mean systolic B.P, mean diastolic B.P, Mean of mean B.P, Mean heart rate 6.Proportion of cases having adverse effects if any in both the groupsTimepoint: 0min 5min 10min 15min 20min 25min 30min 45min 60min 75min 90min	—

Countries

India

Contacts

Public ContactDr Poonam Kalra

SMS medical college jaipur

Nehatewatia94@gmail.com8053075272

Outcome results

None listed

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