Health Condition 1: 4- Measurement and Monitoring
Conditions
Interventions
Control Intervention1: NIL: NIL
Sponsors
Dr Umesh N P
Dr Arunkumaran D
Eligibility
Inclusion criteria
Inclusion criteria: All patients aged between 18 to 60 years posted for elective infraumbilical surgeries ASA physical status grade I and II Patients willing to give informed consent to participate in the study
Exclusion criteria
Exclusion criteria: Patients who are morbidly obese BMI more than 40kg/m2 Patients allergic to study anesthetic drugs Patients shorter than 150cm and taller than 180cm height Patients posted foe emergency surgeries
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the sensory and motor characterstics of clonidine in two different doses when added to intrathecal hyperbaric ropivacaine 0.75% in infraumbilical surgeries. To compare the duration of analgesia of clonidine in two different doses in study subjects.Timepoint: To compare the sensory and motor characterstics of clonidine in two different doses when added to intrathecal hyperbaric ropivacaine 0.75% in infraumbilical surgeries at baseline. To compare the duration of analgesia of clonidine in two different doses in study subjects upto 8hrs | — |
Secondary
| Measure | Time frame |
|---|---|
| To compare the level of sedation, perioperative hemodynamic changes, side effects such as nausea, vomiting, shivering, pruritis, respiratory depression etc in the study subjects.Timepoint: 24 hours | — |
Countries
India
Contacts
Public ContactDr Umesh N P
Mandya institute of medical sciences
Outcome results
None listed