Health Condition 1: N158- Other specified renal tubulo-interstitial diseases
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients aged between 18 and 60 years undergoing urological surgeries. ASA (American Society of Anesthesiologists) Grade I and II patients. Patients willing to provide written informed consent. Patients of either gender who meet the study criteria.
Exclusion criteria
Exclusion criteria: Patients unwilling to participate in the study. ASA Grade III and above patients. Patients with haemorrhagic diathesis or significant scoliosis/kyphosis. Pregnant patients. Patients allergic to the test drugs (clonidine or bupivacaine). Patients with severe comorbid conditions (e.g., uncontrolled hypertension or diabetes). Patients with history of neurological or spinal disorders impacting the administration of spinal anaesthesia.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Onset of sensory block to T10 level and elevation of sensory block to T6 level using pinprick method in patients undergoing urological surgeries.Timepoint: Onset of sensory block to T10 level and elevation of sensory block to T6 level using pinprick method in patients undergoing urological surgeries. | — |
Secondary
| Measure | Time frame |
|---|---|
| Onset and duration of motor and sensory blockade, duration of postoperative analgesia, and hemodynamic stability (heart rate, blood pressure, SpO2).Timepoint: Monitored continuously post-intrathecal injection and at regular intervals intraoperatively and postoperatively until discharge or the first rescue analgesia request. | — |
Countries
India
Contacts
Datta Meghe Institute of Higher Education and Research