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Post operative pain relief in spinal surgeries using epidural anaesthesia

Influence of epidural ropivacaine with or without dexmedetomidine on post operative pain and patient satisfaction after thoracolumbar spine instrumentation: a randomised, comparative study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/01/016906
Enrollment
50
Registered
2019-01-04
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: M484- Fatigue fracture of vertebra Health Condition 2: S320- Fracture of lumbar vertebra Health Condition 3: S220- Fracture of thoracic vertebra Health Condition 4: M858- Other specified disorders of bonedensity and structure Health Condition 5: M844- Pathological fracture, not elsewhere classified Health Condition 6: M480- Spinal stenosis

Interventions

Intervention1: ROPIVACAINE: Will be given via epidural route .1% ropivacaine @5ml/hr for 48 hours Control Intervention1: ROPIVACAINE PLUS dexmedetomidine: Will be given by epidural route .1% ropivac

Sponsors

PGIMER
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA I-III, scheduled for laminectomy, posterior decompression and/or pedicle screw fixation at one or two levels of thoraco-lumbar spine instrumentation

Exclusion criteria

Exclusion criteria: Patient refusal, Mental illness, drug addiction, Renal and hepatic insufficiency, Known allergy to local anaesthetics, Perforation of the dura during surgery, Steroid administration for surgical reasons, Component of cervical spine trauma, Upper limb trauma, head injury

Design outcomes

Primary

MeasureTime frame
To compare the total rescue analgesic consumptionTimepoint: Post operative day 0,1,2

Secondary

MeasureTime frame
Comparison of Patient satisfaction scoresTimepoint: from 0 to 72 hours;To compare the pain intensity by using VAS score at different time interval (every hourly till first 6 hours followed by every 3 hours in next 18 hours and then every 6 hourly till 72 hrs). Timepoint: Every hourly till first 6 hours followed by every 3 hours in next 18 hours and then every 6 hourly till 72 hrs;To compare the time to first rescue analgesia (for keeping VAS less than 4)Timepoint: from 0-72 hours

Countries

India

Contacts

Public ContactFAISAL QURESHI

Post graduate institute of Medical Education and Research

Drshyam.pgi@gmail.com7087003375

Outcome results

None listed

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