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Comparison of drug given either single dose every 5 hourly or continuous infusion pump for postoperative pain relief in bone surgeries

Comparative evaluation of dexmedetomidine ropivacaine bolus VS Dexmedetomidine ropivacaine via elastomeric infusion pump for epidural analgesia in lower limb Orthopaedic surgery - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/071595
Enrollment
80
Registered
2024-07-30
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Health Condition 1: S723- Fracture of shaft of femur Health Condition 2: S822- Fracture of shaft of tibia Health Condition 3: V235- Motorcycle passenger injured in collision with car, pick-up truck or van in traffic accident Health Condition 4: M255- Pain in joint Health Condition 5: R52- Pain, unspecified Health Condition 6: S730- Subluxation and dislocation of hip

Interventions

Intervention1: Epidural analgesia for post operative pain relief in lower limb orthopaedic surgery: Group A - 0.2% Ropivacaine(6ml) + dexmedetomidine(1mcg/kg) bolus Group B- 0.2% Ropivacaine+ dexmede

Sponsors

Dr Supriya Maurya
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1- ASA class 2 and 3 2- Age 18-75 years 3-Patients undergoing lower limb orthopaedic surgery

Exclusion criteria

Exclusion criteria: 1- Infection at injection site. 2-Communication difficulty that would prevent postoperative assessment 3- Any contraindications to epidural anesthesia 4- ASA class 4

Design outcomes

Primary

MeasureTime frame
Primary objective to compare postoperative analgesia in 2 groups with same drug but different delivery method one bolus and other elastomeric infusion pump postoperatively.Timepoint: Primary objective to compare efficacy and quality of postoperative analgesia in 2 groups with same drug but different delivery method one bolus and other elastomeric infusion pump for 48 hours postoperatively.—

Secondary

MeasureTime frame
1-comparison of haemodynamic changes in 2 groups. 2-Any complications of epidural anesthesia 3-Any side effects of drug in the study.Timepoint: For 48 hour.—

Countries

India

Contacts

Public ContactDr Pramod chand

Lala lajpat Rai memorial medical College meerut

pcllrm@gmail.com9557040620

Outcome results

None listed

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