Health Condition 1: null- Patients admitted for lower abdomen and lower limb surgeries
Conditions
Interventions
Intervention1: Clonidine: To study its effect on prolonging the duration of spinal anesthesia using levobupivacaine.
Intervention2: Oral Clonidine: To study the effect of oral clodine premedication on
Sponsors
Self
Eligibility
Inclusion criteria
Inclusion criteria: Patients belonging to ASA I and ASA II class undergoing lower abdominal and lower limb surgeries
Exclusion criteria
Exclusion criteria: 1)History or evidence of coagulopathy and bleeding disorders. 2 )Renal dysfunction 3 )Current use of antiplatelet medication and anticoagulants 4)Any localised infections at the site for spinal anesthesia 5) History of malignancy or coronary artery disease 6)Thromboembolic event and 7)Patient refusal
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To study the effect oral Clonodine premedication on Spinal Anesthesia using LevobupivacaineTimepoint: From the time of Anaesthesia till the time of complete recovery | — |
Secondary
| Measure | Time frame |
|---|---|
| ) Evaluate the effect 1) Evaluate the effect of oral clonidine premedication 2) Compare the combined effect of oral clonidine and levobupivacaine on spinal anes-thesia versus levobupivacaine alone. 3)To study the possible adverse effects of oral clonidine. Timepoint: 24 hours | — |
Countries
India
Contacts
Public ContactDr Radhesh Hegde
Father Muller Medical College
Outcome results
None listed