None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: •Patient who give written informed consent •Patients aged 18 to 60 years. •Patients scheduled for elective infraumbilical surgery. •Patients with ASA (American society of anesthesiologists) grade I & II •Patients with normal haemoglobin values
Exclusion criteria
Exclusion criteria: •Patients refusing to participate in the study. •Patients having ongoing acute infections. •Patients with electrolyte abnormalities. •Patients with hepatic and renal dysfunction. •Patients with chronic alcohol abuse. •Patients with history of endocrine disease inclusive of diabetes mellitis •Morbid obesity, chronic use of steroids or immunosuppressant or recent chemotherapy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| •To assess whether the anaesthetic technique (general anaesthesia and spinal anaesthesia )could affect the neutrophil to lymphocyte ratio after infra umbilical surgeries.Timepoint: at 2hours and 24 hours after surgery | — |
Secondary
| Measure | Time frame |
|---|---|
| To assess whether the anaesthetic technique (general anaesthesia and spinal anaesthesia )could affect the total leukocyte count after infra umbilical surgeries.Timepoint: Total leukocyte count - 3,500-10,500. | — |
Countries
India
Contacts
Bangalore Medical College and Research Institute