Effect of Ketamine+Propofol vs Remifentanyl+Propofol on Laryngeal Mask Insertion Conditions

Ketamine

Brief Summary

Laryngeal mask airway is a common tool for airway management during anesthesia in many surgeries. Insertion of laryngeal mask needs deep anesthesia, suppression of airway, stabile hemodynamic response. Many drug regimens has been used for this purpose. This study aimed to compare the insertion conditions of laryngeal mask by using ketamine+propofol versus remifentanil + propofol.

Intervention / Treatment

Ketamine (DRUG)

To compare ketamine+propofol versus remifentanyl+propofol to maintain good laryngeal mask insertion conditions
remifentanyl (DRUG)

N/A
Propofol (DRUG)

N/A
laryngeal mask (DEVICE)

N/A

Condition or Disease

Surgery

Phase

Study Design

Study type:	OBSERVATIONAL
Status:	Completed
Study results:	No Results Available
Age:	18 Years to 65 Years
Enrollment:	50 (ACTUAL)
Funded by:	Other
Time Perspective:	Prospective
Observational Model:	Case-Control
Masking

Clinical Trial Dates

Start date:	Apr 01, 2015
Primary Completion:	Jan 01, 2016	ACTUAL
Completion Date:	Jan 01, 2016	ACTUAL
Study First Posted:	Oct 22, 2015	ESTIMATED
Results First Posted:	Aug 31, 2020
Last Updated:	May 05, 2017

Sponsors / Collaborators

Lead Sponsor: Ankara University

Responsible Party: N/A

Location

Ankara, Turkey

Cigdem Yildirim Guclu, Ankara, Turkey

Participant Groups

Ketamine+propofol
Remifentanyl+propofol

Eligibility Criteria

Sex:	Female
Minimum Age:	18
Maximum Age:	65
Age Groups:	Adult / Older Adult
Healthy Volunteers:	Yes

Inclusion Criteria:

* Surgery requires laryngeal mask

Exclusion Criteria:

* Patient refusal, abdominal surgery required muscle relaxant, any allergy to ketamine or remifentanyl

Primary Outcomes

High laryngeal mask insertion scores 3 minutes

Secondary Outcomes

Hypotension 10 minutes
Hypertension 10 minutes

More Details

NCT Number:	NCT02583217
Other IDs:	ANK-42476
Study URL:	https://clinicaltrials.gov/study/NCT02583217

Last updated: Sep 29, 2023