Health Condition 1: O80- Encounter for full-term uncomplicated delivery
Conditions
Interventions
None listed
Sponsors
Department of anaesthesiology and critical care PGIMSRohtak
Eligibility
Inclusion criteria
Inclusion criteria: Pregnant females belonging to American Society of Anaesthesiologists (ASA) class I and II, scheduled to undergo lower segment caesarean section under regional anesthesia
Exclusion criteria
Exclusion criteria: � � Any contraindication to regional anesthesia � History of neurological, psychological, or chronic pain disorder � Drug allergy � Refusal to give consent will not be included in the study � Conversion to general anesthesia
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To observe and evaluate the change in perfusion index at following points; Timepoint: a) Time of first request for analgesia b) Thirty minutes after administration of rescue analgesia | — |
Secondary
| Measure | Time frame |
|---|---|
| a) Correlation between perfusion index and visual analogue scale b) Correlation between perfusion index and hemodynamic parameters (HR, MAP) Timepoint: a) evel of block will be recorded as soon as the patient is shifted to recovery room (T0). b) At the time of the first request for analgesia (T1) c) Thirty minutes after analgesic administration (T2) | — |
Countries
India
Contacts
Public ContactPragya Sharma
Pt. B.D sharma institute of medical sciences,PGIMS,rohtak
Outcome results
None listed