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A clinical study to compare two drugs fentanyl and morphine in low dose infusion for pain relief after spine surgeries

Comparison of low dose intravenous fentanyl and morphine infusion for postoperative analgesia in spine surgeries

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/11/010629
Enrollment
100
Registered
2017-11-24
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: M968- Other intraoperative and postprocedural complications and disorders of musculoskeletal system, not elsewhere classified Health Condition 2: null- Patients who are scheduled for spine surgeries are included in the study.

Interventions

Intervention1: Intravenous infusion: The technique in which intravenous canula is started and drug is given by continuous infusion for 24 hours. Control Intervention1: Morphine, Fentanyl: One of the d

Sponsors

SRM Medical College Hospital and Research Centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients with ASA Physical Status I and II posted for spine surgeries 2. Weighing between 50 â?? 100 kg

Exclusion criteria

Exclusion criteria: 1. All patients with ASA Physical Status III and above 2. Patients who refuse to participate in the study 3. Patients who are allergic to opioids 4. Patients who are pregnant 5. Patients with renal, cardiac or hepatic disease 6. Patients with history of obstructive sleep apnea.

Design outcomes

Primary

MeasureTime frame
Total opioid consumptionTimepoint: Amount of opioid consumed to maintain visual analogue pain scale of less than three for 24 hours is noted.

Secondary

MeasureTime frame
Need for oxygenTimepoint: If O2 saturation falls below 94%, oxygen by nasal cannula is given and recorded. If there is further fall in SpO2 or patient becomes apnoeic, then respiration will be assisted by bag and mask ventilation or intubation if needed.;SedationTimepoint: Ramsay sedation score was used to assess the patient sedation level. (1) Anxious, agitated or restless, (2) Oriented, calm and co-operative (3) Responsive to commands only (4) Exhibiting brisk response to light glabellar tap or loud auditory stimulus (5) Exhibiting a sluggish response to light glabellar tap or loud auditory stimulus, (6) Unresponsive.

Countries

India

Contacts

Public ContactRajagopalan Venkatraman

Srm Medical College Hospital and Research Centre

drvenkat94@gmail.com9894581455

Outcome results

None listed

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