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Clinical Trial Details — Status: Unknown status

Administrative data

NCT number NCT01826565
Other study ID # HPPark
Secondary ID
Status Unknown status
Phase N/A
First received March 19, 2013
Last updated May 3, 2013
Start date May 2013
Est. completion date July 2014

Study information

Verified date May 2013
Source Seoul National University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To evaluate the efficacy of rotational technique in the insertion of i-gel


Description:

The i-gel is one of the 2nd generation supraglottic airways. The rotational technique is known to increase the success rate of insertion of other supraglottic airways. The investigators try to evaluate the efficacy of rotational technique in the insertion of i-gel.


Recruitment information / eligibility

Status Unknown status
Enrollment 100
Est. completion date July 2014
Est. primary completion date May 2014
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Patients scheduled for general anesthesia(transurethral resection of bladder tumor or transurethral resection of the prostate) using i-gelTM

Exclusion Criteria:

- History of recent postoperative sore throat

- History of difficult airway

- Mouth opening < 2.5 cm

- Emergency operation

Study Design


Intervention

Procedure:
Rotational technique
90 degree rotation

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Seoul National University Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary The success rate of insertion check oropharyngeal leakage at pressure 12 cmH2O up to 30 min.
Secondary postoperative sore throat severe/moderate/minimal/none up to 2 days
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