Does Laryngoscopic Tecnique Facilitate cLMA Insertion?

Urologic Surgery Clinical Trial

— cLMA  

Official title:

Does Laryngoscopic Tecnique Facilitate cLMA Insertion?

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT02000791
• Other study ID #: laryngeal mask
• Status: Not yet recruiting
• Phase: Phase 4
• First received: November 21, 2013
• Last updated: December 3, 2013
• Start date: December 2013
• Est. completion date: May 2014

Study information

• Verified date: November 2013
• Source: Diskapi Yildirim Beyazit Education and Research Hospital
• Contact: Tugba Arslan, MD
• Phone: +905074378919
• Email: tuba.kokulu[@]gmail.com
• Is FDA regulated: No
• Health authority: Turkey: Ministry of Health
• Study type: Interventional

Clinical Trial Summary

it is compared that laryngeal mask insertion with standard technique and laryngoscopic technique

Description:

Is there any releation between insertion succes rate and difficult intubation criteria. success of the first attempt laryngeal mask insertion, patient response of laryngeal mask placement. And also during the implementation of these two techniques; the effects on heart rate and blood pressure and postoperative complications were investigated.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 180
• Est. completion date: May 2014
• Est. primary completion date: February 2014
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Over 18 age

• under urologic surgery patient

Exclusion Criteria:

• Uper respiratory infection

• Full stomach

• BMI over 40

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Diagnostic

Related Conditions & MeSH terms

• Urologic Surgery

Intervention

Other:
• Comparison of fibreoptic view

Locations

Country	Name	City	State
Turkey	Diskapi Yildiim Beyazit Eduation and Research Hospital	Ankara

Sponsors (1)

Lead Sponsor	Collaborator
Diskapi Yildirim Beyazit Education and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Investigate to easy of insertion whether standart or laryngoscopic technique		1 min after insertion	Yes
Secondary	Fiberoptic view		1 min after insertion	Yes