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OpenTrials
Completed

NCT Number: NCT02583217

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

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.

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Key information

Conditions

Surgery

Age range

18 year–65 year

Sex eligibility

Female

Study type

Observational

Primary location

Cigdem Yildirim Guclu

Ankara, Turkey (Türkiye)

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Surgery requires laryngeal mask

Exclusion criteria

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

Treatment and study plan

ketamine

Drug

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

Other names: Remifentanyl

remifentanyl

Drug

Propofol

Drug

Laryngeal Mask

Device

Primary outcomes

  1. High laryngeal mask insertion scores

    Time frame: 3 minutes

Secondary outcomes

  1. Hypotension

    Time frame: 10 minutes

  2. Hypertension

    Time frame: 10 minutes

Sponsors and collaborators

Lead sponsor

Ankara University

Other

Registry information

Important dates

Study start
2015
Primary completion
2016
Study completion
2016
First posted
Oct 22, 2015
Registry last updated
May 8, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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