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NCT07224620 · ClinicalTrials.gov registry record · Phase 2
Fentanyl Versus Hydromorphone in Patients on Mechanical Ventilation
A Phase 2 study of Mechanical Ventilation and Sedation and Analgesia, sponsored by Beth Israel Deaconess Medical Center.
- Recruiting
- Registry status
- Phase 2
- Development phase
- 300
- Enrollment target
- 1
- Study location
NCT07224620 is a Phase 2 study of Mechanical Ventilation and Sedation and Analgesia that is actively recruiting participants, run by Beth Israel Deaconess Medical Center. The registered enrollment target is 300 participants, below the 576-participant average among 14 other Mechanical Ventilation trials with a reported enrollment target (48% lower). The trial reports 1 study location across 1 state.
The verdict
NCT07224620, a Phase 2 study of Mechanical Ventilation and Sedation and Analgesia, is actively recruiting participants, sponsored by Beth Israel Deaconess Medical Center.
- RECRUITING
- Registry status
- Phase 2
- Development phase
- 300 participants
- Enrollment target
- 1
- Study location
Study Summary
Patients with respiratory failure who require mechanical ventilation are not only at risk of death, but also of complications of prolonged ICU stay. Patients may have significant functional decline, impact in quality of life, develop psychiatric disorders and at long-term can lead to significant cost to society. Although sedation and analgesia are considered only supportive therapy, several studies have shown that in patients on mechanical ventilation, different approaches can have significant impact on patient centered outcomes. However, to date, randomized clinical trials on critically ill patients have mostly evaluated the sedative agent but not the analgesic agent. Although morphine and its derivates are the most common used opioid analgesic agents in the critical care setting, only some retrospective studies and some prospective studies compared them head-to-head (ramifentanyl versus morphine and fentanyl versus morphine). Current guidelines recommend choosing the analgesic agent based on pharmacokinectics, physician experience and side-effects profile. To evaluate the differences of two standard-of-care analgosedation agents, the FenHydro trial will be a cluster randomized, pragmatic, pilot and feasibility superiority clinical trial in mechanically ventilated patients in the ICU. The main question the study hopes to answer is whether there is any difference in morphine milligram equivalents administered during mechanical ventilation.
Conditions Studied
Interventions
- DRUG fentanyl
- DRUG Hydromorphone
Study Locations (1)
Massachusetts
- Beth Israel Deaconess Medical Center - Boston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 300 participants |
| Start Date | 2025-11 |
| Est. Completion | 2026-06 |
| Phase | Phase 2 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07224620
The ClinicalTrials.gov registry entry for NCT07224620 describes a study currently listed as recruiting, categorized as Phase 2. The registered enrollment target is 300 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 576-participant average among 14 other Mechanical Ventilation trials with a reported enrollment target (48% lower). The listed sponsor is Beth Israel Deaconess Medical Center, which has 488 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Mechanical Ventilation appearing as the primary indexed condition, and to 2 interventions - of which fentanyl is the first listed.
NCT07224620 reports 1 study location spanning 1 distinct geographic area - top geographies include Massachusetts.
Frequently Asked Questions
What is clinical trial NCT07224620 about?
NCT07224620 is a clinical study titled "Fentanyl Versus Hydromorphone in Patients on Mechanical Ventilation". Patients with respiratory failure who require mechanical ventilation are not only at risk of death, but also of complications of prolonged ICU stay. Patients may have significant functional decline, impact in quality of life, develop psychiatric disorders and at long-term can lead to significant cos...
What is the current status of trial NCT07224620?
This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 300 participants. The study started on 2025-11. Estimated completion is 2026-06.
What conditions does trial NCT07224620 study?
This clinical trial studies the following conditions: Mechanical Ventilation, Sedation and Analgesia, Critical Care, Intensive Care.
What interventions are being tested in trial NCT07224620?
The interventions under investigation include: fentanyl (DRUG), Hydromorphone (DRUG).
Who is sponsoring clinical trial NCT07224620?
This trial is sponsored by Beth Israel Deaconess Medical Center, which has 488 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07224620 being conducted?
This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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