Health Condition 1: C719- Malignant neoplasm of brain, unspecified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: With body mass index (BMI) of 18.5– 29.9 kg/m2, belonging to ASA physical status of 1 or 2, scheduled for elective awake craniotomy
Exclusion criteria
Exclusion criteria: Refusal of the patient Pregnancy, bleeding disorder Patients receiving sedatives Psychological disturbances Alcohol or substance abuse Presence of cardiac or respiratory disease ? Local infection at site of injection ? Patients with known allergy to any of the study drugs ? Coagulopathy ? Hepatic or Renal impairment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the time interval of the the first dose of rescue analgesia during perioperative period. (Defined as the duration between onset of sensory blockade to the first use of rescue analgesic drug as demanded by the patient (NRS = 4). Timepoint: Till 24 hrs | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. To compare the time needed for onset of sensory block (will be checked by loss of pin prick sensation at every 2 min). 2.To see intraoperative hemodynamic response after adding adjuvants to ropivacaine in scalp block, measured using HR & MAP. 3.Incidence of intra operative & 24hr post operative pain measured using NRS score. 4.Total consumption of rescue analgesic drug in 24 hrs postoperatively. 5.Intraoperative & postoperative complications such as nausea, vomiting, oversedation, respiratory depression, bradycardia, hypotension, failure of block, conversion to GA will be recorded. Timepoint: Till 24 hrs | — |
Countries
India
Contacts
Post Graduate Institute of Medical Education and Research, Chandigarh