CI

At a glance

ClinicalIndex Comparison Record
N/AActive· 120 target
Drug / intervention
Nebulized fentanyldrug
Likely dose
Nebulized fentanyl 2 mcg/kgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06689124
NCT06689124N/AActiveUpdate OverdueUpdated 19mo ago · Completion was 12mo ago
Enrollment Stalled

A Randomized Study Comparing of Three Doses Nebulized Fentanyl in Older Adults With Severe Musculoskeletal Pain at the Emergency Department

Bangkok Metropolitan Administration Medical College and Vajira Hospital·interventional·Posted Nov 14, 2024·Updated Nov 14, 2024

In Brief

A clinical study evaluating Nebulized fentanyl for Treatment Side Effects and Musculoskeletal Pain. Active but no longer recruiting, targeting 120 participants across 2 sites.

Signals

Enrollment appears stalled

Detailed Summary

This clinical trial compares three different nebulized fentanyl dosages for older persons experiencing severe musculoskeletal pain at the emergency department. The main objective is: Does the effectiveness of nebulized fentanyl at dosages of 2 mcg/kg, 3 mcg/kg, and 4 mcg/kg at 30 minutes differ in older patients who report to the emergency room with pain from musculoskeletal injuries? Secondary outcome are: 1. Incidence of adverse effects after drug administration at minutes 0, 15, 30, 45, 60, 75, 90, 105, 120 2. Incidence of receiving other pain relief treatments (rescue therapy) in minutes 30, 45, 60, 75, 90, 105, 120 Participants will receive an explanation of the study and possible side effects, which may take approximately 5-10 minutes, without affecting the primary treatment of the patients. Consent will be obtained in this study, along with signing or fingerprinting as evidence in the consent form.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesThailand

Timeline

N/AActiveOverdue
20252026
First PostedNov 14, 2024
Enrollment StartJul 1, 2024
Primary CompletionJul 1, 2025
TodayJul 2, 2026
Enrollment to primary: 1 yearPosted 1.6 years ago

Interventions

Nebulized fentanyldrug

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.