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To study the effect of xylocaine on intraocular pressure during intubatio

Not Applicable
Conditions
Health Condition 1: O- Medical and Surgical
Registration Number
CTRI/2023/10/058197
Lead Sponsor
Department of anesthesiology and critical care
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1.Belong to ASA class I and II

2.Weight ranging from 45-60 kg

3.Non-ophthalmic surgeries

Exclusion Criteria

1. Anticipated difficult airway

2.history of hypertension

3. Treatment with beta blockers and calcium channel blockers or any other drug causing hemodynamic instability

4. Laryngoscopy time more than 30 seconds

5. Allergic to Xylocaine

5.pregnant and lactating mothers

6. Patients refusal to participate in study

7. Ophthalmic surgeries

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To determine the changes on intraocular pressure (IOP) after giving 2% intravenous xylocaine.Timepoint: Intraocular pressure (IOP) will be measured by Perkins tonometer at pre induction baseline immediately after intubation & 1 3 5 & 15 minutes after that
Secondary Outcome Measures
NameTimeMethod
To determine the hemodynamic changes due to 2% intravenous xylocaine during endotracheal intubation.Timepoint: Heart rate today Systolic blood pressure, Diastolic blood pressure & Mean Blood Pressure ) will be measured by monitoring at pre induction (baseline), immediately after intubation and 1,3,5 and 15 minutes after that.
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