A study to check the safety and feasibility of Laryngeal Mask Airways with wide gastric port for Trans-esophageal Echocardiography guided cardiac catheterisation procedures.
Not Applicable
Completed
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2022/12/047811
- Lead Sponsor
- Dr Sanjeeta Rajendra Umbarkar
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 30
Inclusion Criteria
I.Patients posted for percutaneous device closure procedures under TEE guidance.
II.Mouth opening >35mm.
III.Mallampati score 1or2
IV.Weight >30 kg.
V.Strict NBM.
Exclusion Criteria
I.Hemodynamically unstable.
II.Patient at risk of aspiration.
III.Difficult intubation.
IV.Edentulous.
V.Surgery duration >3hrs.
VI.Significant acute or chronic lung disease
VII.Known airway problems.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To check feasibility and safety of second generation LMA with wide gastric port in ease of TEE probe placement and efficient airway management of patients in percutaneous device closure procedures requiring TEE.Timepoint: From start of procedure to 24hrs post procedure in ICU.
- Secondary Outcome Measures
Name Time Method 1)To observe success rate of TEE probe insertion. <br/ ><br>2)To observe success rate of LMA insertion. <br/ ><br>3)To observe ease of LMA insertion. <br/ ><br>4)To note presence of sore throat after LMA removal. <br/ ><br>5)To note visualisation of blood on the LMA after removal. <br/ ><br>6)To note any airway compromise after LMA removal. <br/ ><br>7)To note post-operative laryngospasm <br/ ><br>8)To note damage to Trans esophageal echocardiography probe.Timepoint: From start of procedure to 24hrs post procedure in ICU.