Health Condition 1: - Health Condition 2: O- Medical and Surgical
Conditions
Interventions
Intervention1: Preservative free Ketamine: Addition of preservative free 25 mg(0.5ml)ketamine for spinal anaesthesia with either of the three-0.5% hyperbaric bupivacaine,0.5% hyperbaric ropivacaine an
Sponsors
Bharati Vidyapeeth deemed to be university medical college and hospital
Eligibility
Inclusion criteria
Inclusion criteria: Age 18-65 years, both genders, American Society of Anesthesiologists (ASA) Grading, I-II, posted for the lower abdominal (below umbilicus)/pelvic and lower limb surgical procedures planned under subarachnoid block will be included in the study.
Exclusion criteria
Exclusion criteria: 65 years, non-consenting as well as pregnant patients, patients with uncontrolled co-existing systemic or metabolic diseases, history of alcohol or substance abuse, known sensitivity to any of the LAAS or ketamine shall be excluded from the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To study and compare the efficacy of intraoperative and postoperative analgesia produced by addition of preservative-free ketamine to the hyperbaric preparations of bupivacaine, ropivacaine and levobupivacaine administered via subarachnoid block.Timepoint: 6 months | — |
Secondary
| Measure | Time frame |
|---|---|
| To study and compare the haemodynamic effects of addition of preservative-free ketamine to the hyperbaric preparations of bupivacaine, ropivacaine and levobupivacaine administered via subarachnoid block. To study and compare any side effects/complications addition of preservative-free ketamine to the hyperbaric preparations of bupivacaine, ropivacaine and levobupivacaine administered via subarachnoid block.Timepoint: 6 months | — |
Countries
India
Contacts
Public ContactDrNeha Tilak
Bharati Hospital Deemed to be University and Medical college
Outcome results
None listed