Health Condition 1: M859- Disorder of bone density and structure, unspecified Health Condition 2: O- Medical and Surgical
Conditions
Interventions
Intervention1: 0.75% hyperbaric Ropivacaine 3ml + dexmedetomidine 5 mcg: After adequate preoperative evaluation, patient will be brought inside operation theatre.Blood pressure, ECG leads, pulse oxime
Sponsors
Dr Soumya Patted
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients of age group 18-60 years undergoing infraumbilical surgeries under supbarchnoid block. 2. Patients willing to give written informed consent 3. Patients belonging to ASA I and II
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1) To compare the block characteristics of intrathecal Dexmedetomidine versus Clonidine as an adjuvant to 0.75% Hyperbaric Ropivacaine in terms of the onset and duration of sensory block and motor block 2) To compare the duration of post operative analgesiaTimepoint: From time of intrathecal injection to every 30 seconds till the loss of sensation at T10 dermatomal level and thereafter at 2 mins intervals till the maximum level of sensory blockade is achieved and subsequently at 30 mins interval until complete recovery. From time of intrathecal injection every 1 minute for the first 5 min, then at 5-min intervals for next 30 minutes and at every 30 minutes intervals until complete resolution of motor anesthesia. | — |
Secondary
| Measure | Time frame |
|---|---|
| to compare effects of dexmedetomidine and clonidine on hemodynamic parameters, sedation and adverse effects. Timepoint: Before spinal anaesthesia, after spinal anaesthesia every 2 minutes for first 10 minutes, then every 5 minutes for 30 minutes, thereafter every 10 minutes till end of surgery . Immediate post operative period, every 2 hours for 6 hours, 12 hours and 24 hours | — |
Countries
India
Contacts
Public ContactDr Samudyatha T J
Bangalore Medical College and Research Institute
Outcome results
None listed