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Compare the effect of Intraoperative infusion of Remifentanil versus Fentanyl on pain management post operatively in patients undergoing spine surgery under general anaesthesia

Comparison of effect of Intraoperative infusion of Remifentanil versus fentanyl on post-op pain management in patients undergoing elective spine surgery under general anaesthesia - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/069025
Enrollment
46
Registered
2024-06-18
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

Health Condition 1: O- Medical and Surgical Health Condition 2: M958- Other specified acquired deformities of musculoskeletal system

Interventions

Intervention1: Remifentanyl: Remifentanyl is an ultra-short acting opioid that facilitates hemodynamic and neurologic management. Owing to its short half life it is preferred as an infusion. Postopera

Sponsors

JNMC
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient giving informed consent No history of substance abuse BMI more than thirty-five ASA grade one, two, three Patients posted for spine surgery

Exclusion criteria

Exclusion criteria: Patients not willing to participate in the study BMI more than thirty-five ASA grade four and above Patients who received opioids within two days prior to surgery Known hypersensitivity to opioids Pregnant females

Design outcomes

Primary

MeasureTime frame
Remifentanyl is better alternative to Fentanyl in pain management in spine surgery patientsTimepoint: 24 hrs

Secondary

MeasureTime frame
1. Comparison of hemodynamic parameters during intraoperative & postoperative period 2. Assessment of postoperative opioid consumption 3. evaluation of postoperative nausea & vomiting 4. compare total amount of rescue analgesics (IV Tramadol) used during 24 hour postoperative period 5. study side effects & complications during postoperative periodTimepoint: 24 hrs

Countries

India

Contacts

Public ContactNeeta Chaudhary Verma

Datta Meghe Institute of Medical Science and research

neetachaudhary1234@gmail.com8788378382

Outcome results

None listed

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