Health Condition 1: null- Patients undergoing abdominal and vaginal hysterectomy
Conditions
Interventions
Intervention1: Group BP: Intrathecal Bupivacaine heavy 3ml and normal saline 0.1ml
Control Intervention1: Group BC
: Intrathecal Bupivacaine heavy 3ml and clonidine 15micrograam 0.1ml
Control Interv
Sponsors
Suart municiple institute of medical college and research
Eligibility
Inclusion criteria
Inclusion criteria: 90 patients between the age group 18 to 75years belonging to ASA physical status class I and II schedule for surgeries below umbilicus.
Exclusion criteria
Exclusion criteria: Contraindications for regional anesthesia including absolute refusal by patient, severe hypovolemia, coagulopathy, infection at site of injection, valvular heart diseases, patients with history of sensitivity to study drugs.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the onset and duration of sensory and motor blockade following intrathecal Bupivacaine supplemented with either Dexmedetomidine or Clonidine.Timepoint: Just after giving spinal anaesthesia sensory block checked by pin prick method and motor block by modified bromage score | — |
Secondary
| Measure | Time frame |
|---|---|
| Assess the haemodynamic stability postoperative analgesia requirement Any side effects in all groups perioperatively. Timepoint: Resque analgesic requirement by VAS score at postoperative 1,2,3,4,6,8,10,12,14,16,20 and 24hr Sedation by Five point sedation score intraoperatively and postoperatively upto 24hr Pulse,blood pressure and respiratory rate intraoperative and postoperative upto 24hr | — |
Countries
India
Contacts
Public ContactHetal Hathiwala
Surat municiple institute of medical college and research
Outcome results
None listed