Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Control Intervention1: Intrathecal Ropivacaine plus Clonidine: In this group 3 ml of 0.75% hyperbaric Ropivacaine + 30 ug of clonidine in 0.5ml normal saline. Total volume 3.5ml will be given intrathe
Sponsors
Dr Shruti Desai
Eligibility
Inclusion criteria
Inclusion criteria: ASA grade I and II BMI Patients who have given written informed consent. Patients undergoing elective infraumbilical surgeries under spinal anaesthesia
Exclusion criteria
Exclusion criteria: 1.ASA grade III and IV 2.Patients with known psychiatric illness, chronic pain or any condition that precludes intrathecal anesthesia. 3.Patients with deformity of the spine. 4.Patients with skin infection at the site of anesthesia. 5.Known sensitivity or allergy to the study drugs 6.Patients on chronic anticoagulants or antit platelet drugs or patients with coagulopathy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the onset and duration of sensory and motor blockade and duration of postoperative analgesiaTimepoint: The effects will be assessed at baseline,5,10,15, 20,25,30,60,90,120,150,180 minutes after giving spinal anesthesia.Postoperatively the analgesia effect will be assessed at baseline, 1,2,3,4,5,6,12 and 24 hours postoperatively. | — |
Secondary
| Measure | Time frame |
|---|---|
| to assess perioperative hemodynamic stability and incidence of side effectsTimepoint: The hemodynamic stobility and adverse effects will be assessed intraoperatively at baseline,5,10,15, 20,25,30,60,90,120,150,180 minutes after giving spinal anesthesia. And Postoperatively it will be assessed at baseline, 1,2,3,4,5,6,12 and 24 hours postoperatively. | — |
Countries
India
Contacts
Public ContactDr Shruti Desai
GCS medical college, hospital and research centre
Outcome results
None listed