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A clinical study to compare two different techniques to decrease the length of hospital stay and postoperative pain relief after spine surgeries

Comparison of Multimodal Analgesia with Patient Controlled Morphine Analgesia for Enhanced Recovery after Spine Instrumentation Surgeries â?? A Randomised Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/03/050749
Enrollment
60
Registered
2023-03-16
Start date
Unknown
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

Health Condition 1: M958- Other specified acquired deformities of musculoskeletal system

Interventions

Intervention1: Multimodal drugs: Multiple non opioid drugs will be given through oral route preoperatively and postoperatively. T.para 650mg OD T.gabapentin 150mg OD T. baclofen 10mg OD T.ketorolac 30

Sponsors

SRM Medical college Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.ASA I and II 2.Patients scheduled for Single segment spine instrumentation surgeries

Exclusion criteria

Exclusion criteria: 1.Diabetes mellitus 2.Patients with cardiac, renal, liver diseases. 3.Patient taking opioids preoperatively. 4.Uncooperative patients

Design outcomes

Primary

MeasureTime frame
To compare the length of hospital stay between the two groups Timepoint: within 7 days of surgery—

Secondary

MeasureTime frame
Incidence of adverse effects like urinary retention, nausea, vomiting, pruritus Timepoint: 48h after surgery;To compare incidence of readmission after dischargeTimepoint: post discharge till 3 months;To compare Postoperative analgesiaTimepoint: 48h after surgery—

Countries

India

Contacts

Public ContactYazhini

Srm Medical College Hospital and Research Institute

drvenkat94@gmail.com9894581455

Outcome results

None listed

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