CompletedPhase 4ketamine

Use of Ketamine for Conscious Sedation in Flexible Bronchoscopy

Sponsored by Brooke Army Medical Center

NCT ID
NCT06181188
Target Enrollment
66 participants
Start Date
2019-07-15
Est. Completion
2023-10-30

About This Study

In this study, the investigators plan to conduct a single blinded randomized controlled trial in the Pulmonary Service to demonstrate the efficacy of ketamine and its utility in moderate sedation. Patients presenting for bronchoscopy who meet inclusion criteria will be approached, and if amenable, will be consented and enrolled. Patients will be randomized to receive either 1 mg of midazolam and ketamine 0.25 to 0.5 mg/kg loading dose with subsequent doses of 10-20 mg IV or standard fentanyl and midazolam in 25mcg and 1mg increments respectively for moderate sedation during their procedure. The primary outcome will be patient satisfaction, which will be measured a using patient clinical satisfaction form. A number of secondary outcomes will include the following: (1) provider satisfaction (2) the time from sedation administration to procedure start (when the scope is inserted), (3) the time from sedation to scope removal from the trachea (4) the time from sedation to discharge (defined as the time from the end of the procedure until the patient meets discharge criteria from the recovery area), (5) total dose of medications given (including midazolam, fentanyl, and ketamine), (6) adverse events, (7) vital signs, (8) and the need for additional medications, in particular reversal agents.

Conditions Studied

Conscious SedationPatient SatisfactionKetamine

Interventions

  • Ketamine
  • Midazolam
  • Fentanyl

Eligibility

Age:18 Years - 75 Years
Healthy Volunteers:Yes
View full eligibility criteria
Inclusion Criteria:

* Patients age 18 to 75 years who present to the pulmonary clinic for bronchoscopy and considered for airway survey, transbronchial biopsy, endobronchial biopsy, or bronchoalveolar lavage.
* Provider performing the bronchoscopy

Exclusion Criteria:

* Systolic blood pressure over 180mmHg and/or diastolic blood pressure over 110 on two consecutive readings
* Tachycardia greater than 120 beats/minute on two consecutive measurements
* Any allergy to ketamine, fentanyl, or midazolam
* Patient is pregnant or refuses pregnancy test,in women of child-bearing potential\*
* American Society of Anesthesiologists (ASA) score \> 3
* Presence of a history of psychosis, hallucinations, and/or a psychotic disorder

Study Locations (1)

Brooke Army Medical Center
San Antonio, Texas, United States

This trial is not recruiting

This study has completed enrollment. Check back for results or find similar trials.

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Data Source
ClinicalTrials.gov

Last updated from source