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Comparison of the effect of depressive symptoms on the dose requirement during the start of anesthesia in patients undergoing surgery for cancerous and other non-cancerous conditions - A Prospective Observational Study

Not Applicable
Conditions
Health Condition 1: C00-D49- Neoplasms
Registration Number
CTRI/2020/08/027213
Lead Sponsor
JIPMER Intramural fund
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Age > 18 years.

2.American Society of Anaesthesiologists (ASA) physical status I, II, and III.

3.Patients undergoing elective surgery for malignant and non-malignant non-neurological conditions.

Exclusion Criteria

1.Severe cardiovascular compromise or an ejection fraction of 20%.

2.Allergy to Propofol . 3. Modified Mallampatti Score 3 or more.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To compare the difference in propofol required for induction of anesthesia in patients undergoing surgery for malignancy versus those undergoing surgery for non-malignant conditionsTimepoint: Dose required to attain a BIS value between 50-60 at the time of induction
Secondary Outcome Measures
NameTimeMethod
To compare the amount of inotrope/ vasopressor/ anesthetic agent/ opioid required to restore the altered hemodynamic response associated with induction, laryngoscopy and intubation in patients undergoing surgery for malignancy versus those undergoing surgery for non-malignant conditions.Timepoint: 2,4,6,8,10 minutes;To record the hemodynamic response at the time of induction, laryngoscopy and intubation in patients undergoing surgery for malignancy versus those undergoing surgery for non-malignant conditions.Timepoint: 2.4.6.8.10 minutes;3.To compare the difference in propofol required for induction of anesthesia in patients undergoing surgery for malignancy with a PHQ-9 score more than 9 versus those undergoing surgery for malignancy with a PHQ-9 score less than or equal to 9.Timepoint: Dose required to attain a BIS value between 50-60 at the time of induction
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