A Randomized Study Comparing of Three Doses Nebulized Fentanyl in Older Adults

NAActive, not recruitingINTERVENTIONAL
Enrollment

120

Participants

Timeline

Start Date

July 1, 2024

Primary Completion Date

July 1, 2025

Study Completion Date

July 1, 2025

Conditions
Treatment Side EffectsMusculoskeletal Pain
Interventions
DRUG

Nebulized fentanyl

After the enrollment process, the main research assistant will take a brown envelope containing the randomization and hand it to the principal investigator in numerical order. The principal investigator will then open the envelope to determine the group assignment for the patient, revealing which fentanyl nebulization dosage group (2 mcg/kg, 3 mcg/kg and 4 mcg/kg) the patient will be placed in. In this study, participants will be divided into three groups as previously described. We evaluate pain score at 0, 15, 30, 45, 60, 75, 90, 105 and 120 minutes after receiving nebulized fentanyl by a train research assistance who is blind from the treatment dosage.

Trial Locations (2)

10300

Faculty of Medicine,Vajira Hospital, Bangkok

Jiraporn Sri-on, Bangkok

All Listed Sponsors
collaborator

Navamindradhiraj University

OTHER

lead

Bangkok Metropolitan Administration Medical College and Vajira Hospital

OTHER_GOV

NCT06689124 - A Randomized Study Comparing of Three Doses Nebulized Fentanyl in Older Adults | Biotech Hunter | Biotech Hunter