Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients willing to participate in the study Patients in ASA Grade I & II Patients willing to give written informed consent
Exclusion criteria
Exclusion criteria: Patientâ??s refusal to participate in the study. Patients with haemorrhagic diathesis. ASA Grade III and above Patients having allergy to test drug Patients with significant scoliosis or kyphosis Pregnant patients
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| comparision of post operative analgesia in patients receiving bupivacaine with fentanyl and Ropivacaine with fentanyl in lower limb orthopaedic surgeries via Sub arachnoid blockTimepoint: Postoperative 24 hours | — |
Secondary
| Measure | Time frame |
|---|---|
| comparision of haemodynamic parameters & side effects if anyTimepoint: post operative 2 hours | — |
Countries
India
Contacts
DATTA MEGHE INSTITUTE OF HIGHER EDUCATION AND RESEARCH