Skip to main content
Clinical Trials/CTRI/2024/06/069194
CTRI/2024/06/069194
Not yet recruiting
Phase 4

Comparison of analgesic efficacy of pre-emptive paracetamol, ibuprofen and paracetamol-ibuprofen in orthopedic surgeries. - NI

Government Medical College and Hospital0 sites0 target enrollmentTBD

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Not specified
Sponsor
Government Medical College and Hospital
Status
Not yet recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Interventional

Investigators

Sponsor
Government Medical College and Hospital

Eligibility Criteria

Inclusion Criteria

  • Inclusion criteria
  • 1 ASA class I or II
  • 2 Age from 18 to 70 years either sex
  • 3 Measuring 150 to 180 cm height, with body mass index BMI of 18 to 35 kg per m2
  • 4 Patients undergoing elective and emergency orthopaedic surgeries requiring spinal anaesthesia

Exclusion Criteria

  • 1 All contraindications to spinal analgesia including bleeding diathesis, infection at the puncture site, spinal deformity, patient on anticoagulants, pre existing neurological deficits in lower extremities, unwillingness to give consent.
  • 2 Surgical duration more than 2 hours
  • 3 Sensory blockade inadequate for surgery.
  • 4 Patients having cardiac rhythm abnormalities.
  • 5 History of alcoholism, drug abuse, and psychiatric disorders.
  • 6 History of allergy to any of the study drugs.
  • 7 Hepatic disease, renal disease, cardiopulmonary disease, hypertension, diabetes, central or peripheral nervous system disorders.
  • 8 Chronic pain patients undergoing treatment with opioid analgesic.
  • 9 Pregnant patients.

Outcomes

Primary Outcomes

Not specified

Similar Trials