A study of type of anaesthetic techniques in patients with acyanotic congenital heart diseases undergoing device closure

Not Applicable

• Conditions: Health Condition 1: null- Patients with congenital acyanotic heart diseases undergoing device closure

• Registration Number: CTRI/2017/11/010360
• Lead Sponsor: okmanya Tilak Municipal Medical College and General Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2017-07-13
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 80

Inclusion Criteria

All patients of above mentioned age group having acyanotic congenital heart disease undergoing device closure under general Anaesthesia

Exclusion Criteria

Haemodynamically unstable patients

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To study the safety of type of Anaesthesia in various defects like ASD VSD and PDA by studying the incidence of airway related complications like laryngospasm bronchospasm occurring intraoperatively or in the postoperative period and monitoring the incidence of device dislodgement related to anaesthesia technique induced complicationsTimepoint: 1 two minutes after injection of induction drug <br/ ><br>2 Airway related complications like laryngospasm, bronchospasm occurring within 30 to 60 seconds after intubation <br/ ><br>3 Incidence of device dislodgement occurring 5 min to 24 hours after placement of device

Secondary Outcome Measures

Name	Time	Method
Study of other device related complications like Arrhythmias, Perforation of major vessels, difficulty in placement of deviceTimepoint: Intraoperatively every ten minutes