Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Intervention1: Group R: Patients proposed to undergo transurethral resection of the prostate under spinal anesthesia using hyperbaric ropivacaine 0.75 percent 2.8 ml plus fentanyl 15 mcg.
Control Inte
Sponsors
Government Institute Of Medical Sciences
GOVERNMENT INSTITUTE OF MEDICAL SCIENCES
Eligibility
Inclusion criteria
Inclusion criteria: 1. Adult patients aged between 55-80 years, 2. American Society of Anesthesiologists (ASA) grade1 and grade2 3. Scheduled for elective surgery under spinal anesthesia 4. No history of allergy or sensitivity to any of the studied local anesthetics.
Exclusion criteria
Exclusion criteria: 1.Patients have significant cardiovascular disease, Hypertension, renal failure, hepatic dysfunction, and chronic pulmonary disease. 2. Neuromuscular disorder 3. Morbid obesity 4. Bleeding disorders 5. Infection at the local site 6. Any patient on prolonged drug therapy 7. Uncooperative patients
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Comparison of clinical efficacy of hyperbaric ropivacaine with hyperbaric bupivacaine in spinal anaesthesiaTimepoint: To compare the efficacy in terms of hemodynamic stability & duration of motor block until return to normal function | — |
Secondary
| Measure | Time frame |
|---|---|
| 1The total duration of sensory blockade 2Total duration of analgesiaTimepoint: 1 The total duration of sensory blockade will be defined as the time interval between spinal anesthesia till block regression to S2 segment. 2 Duration of analgesia will be defined as time interval from subarachnoid injection to the point where patients demanded rescue analgesics for pain relief and3. any adverse effects. | — |
Countries
India
Contacts
Public ContactDr Savita Gupta
Government Institute Of Medical Sciences
Outcome results
None listed