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

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02583217

Enrollment

Registered

2015-10-22

Start date

2015-04-30

Completion date

2016-01-31

Last updated

2017-05-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Surgery

Keywords

Laryngeal mask, Ketamine, Remifentanyl

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.

Interventions

DRUGKetamine

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

DRUGremifentanyl

DRUGpropofol

DEVICElaryngeal mask

Study design

Observational model

CASE_CONTROL

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

FEMALE

Age

18 Years to 65 Years

Healthy volunteers

Inclusion criteria

* Surgery requires laryngeal mask

Exclusion criteria

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

Design outcomes

Primary

Measure	Time frame
High laryngeal mask insertion scores	3 minutes

Secondary

Measure	Time frame
Hypotension	10 minutes
Hypertension	10 minutes

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026