Comparison of Nebulized Ketamine With Nebulized Magnesium Sulfate for the Prevention of Postoperative Sore Throat

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorSohag University

About this trial

The aim of this study is to compare the efficacy of nebulized ketamine versus nebulized magnesium sulfate in reducing the incidence and severity of POST.

* Primary outcome

• To compare the incidence of POST method. * Secondary outcomes

* Onset, Severity, and duration of POST at 0, 2, 4, 6, 12, 24 hours postoperative. * The hemodynamics recording (HR, BP, MBP, pre and post nebulization) * Adverse Effects (e.g., sedation, cough, nausea, vomiting, ….)

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Age from 18 to 65 years old.

Both sexes.

American Society of Anesthesiologists (ASA) physical status I-II.

Elective surgery requiring GA with endotracheal intubation.

Disqualifiers

Surgery involves the oral cavity, nasopharynx, larynx, and neck regions.

Surgery requires prone position.

Surgery lasted more than 3 hours.

History of preoperative sore throat, common cold.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Ketamine nebulizer

    Drug

    50 patients will receive preoperative nebulization with 50 mg ketamine in 5 ml normal saline.

  • Mg sulfate nebulizer

    Drug

    50 patients will receive preoperative nebulization with 250 mg magnesium sulfate in 5 ml normal saline.

  • Placebo

    Drug

    50 patients will receive preoperative nebulization with 5 ml normal saline.

Treatment groups

150 Participants
are divided into 3 treatment groups
Group A: Ketamine groupExperimental treatment 1 intervention
Group B: Mg sulfate groupExperimental treatment 1 intervention
Group C: Placebo groupPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

To compare the incidence of Post operative sore throat method.

Time frame
24 hours

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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