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A study comparing two methods of transoesophageal echocardiography probe insertion in patients undergoing cardiac surgery

To compare video laryngoscopy versus conventional blind technique for transoesophageal echocardiography probe insertion in patients undergoing cardiac surgery: A randomized controlled study - N/A

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/06/112761
Enrollment
104
Registered
2026-06-15
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: I978- Other intraoperative and postprocedural complications and disorders of the circulatory system, not elsewhere classified

Interventions

Intervention1: Video laryngoscope guided TEE probe insertion: Patients will undergo transoesophageal echocardiography (TEE) probe insertion under direct visualization using a video laryngoscope. Probe

Sponsors

AIIMSPatna
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA physical status I to III Age 18-70 years, Patients posted for elective open-heart surgery with H/O coronary artery diseases

Exclusion criteria

Exclusion criteria: Patient refusal to participate in the study, BMI more than 35, Unanticipated difficult airway, Hemodynamically unstable, Cognitive dysfunction

Design outcomes

Primary

MeasureTime frame
To compare the incidence of oropharyngeal injury after TEE probe insertion using two different techniques ( Blind versus VLs guided) in patients undergoing elective cardiac surgeryTimepoint: baseline after end of surgery

Secondary

MeasureTime frame
The number of attempts require for successful TEE probe insertion, The duration of insertion and the relationship between laryngeal and esophageal inlet Timepoint: at the end of surgery

Countries

India

Contacts

Public ContactDr Shashi Kant

AIIMS,Patna

dr.shashikant2000@gmail.com09934221343

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026