Effect of Induction Method in Post Operative Agitation

Emergence Agitation Clinical Trial

Official title:

the Effect of Two Different Method; Mask Ventilation or Intravenous Canulation on Emergence Agitation and Recovery Conditions on Pediatric Adenotonsillectomy

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03252405
• Other study ID #: emergence agitation
• Status: Completed
• Phase: N/A
• Start date: August 2, 2017
• Est. completion date: October 30, 2017

Study information

• Verified date: September 2019
• Source: Ahi Evran University Education and Research Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To compare the effect of two different induction method; mask ventilation and intravenous cannulation on emergence agitation on pediatric adenotonsillectomy

Description:

Many things cause emergence agitation after operations on pediatric population. This research aims determine which method, mask ventilation or intravenous cannulatin is more effective on emergence agitation

Recruitment information / eligibility

• Status: Completed
• Enrollment: 67
• Est. completion date: October 30, 2017
• Est. primary completion date: October 30, 2017
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 2 Years to 12 Years

Eligibility

Inclusion Criteria:

• pediatric adenotonsillectomy

Exclusion Criteria:

• patients with neurological, hepatic, renal disorders and using any drugs

Related Conditions & MeSH terms

• Emergence Agitation
• Emergence Delirium
• Psychomotor Agitation

Intervention

Device:
• mask ventilation
before intravenous induction, mask application is made. then intravenous cannulation and induction
• intravenous cannulation
induction is applied by using intravenous cannulation

Locations

Country	Name	City	State
Turkey	Diskapi Yildirim Beyazit Education and research hospital	Ankara
Turkey	Ahi evran university education and research hospital	Kirsehir

Sponsors (1)

Lead Sponsor	Collaborator
Ahi Evran University Education and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	assess changing in pediatric agitation/ emergence delirium scale(PAED) scores	to asses change of intensity of postoperative emergence agitation/ delirium (PAED) by using pediatric agitation emergence delirium scale with scores. to assess changing PAED scores at one hour after transfer into the post anesthesia care unit.	postoperative first hour
Secondary	FLACC (face, legs,activity, cry, consolobility)	to asses postoperative pain intensity with scores by FLACC (face, legs,activity, cry, consolobility) scale after transfer into the post anesthesia care unit	postoperative first hour