Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00654329 · ClinicalTrials.gov registry record · Phase 4

Dexmedetomidine vs Fentanyl for BMT

A Phase 4 study, sponsored by Children's National Research Institute.

Completed
Registry status
Phase 4
Development phase
101
Enrollment target

NCT00654329: Completed Phase 4 study, sponsored by Children's National Research Institute.

NCT00654329 is a Phase 4 study that has completed, run by Children's National Research Institute. The registered enrollment target is 101 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (81% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00654329, a Phase 4 study, has completed, sponsored by Children's National Research Institute.

COMPLETED
Registry status
Phase 4
Development phase
101 participants
Enrollment target

Study Summary

A randomized controlled clinical trial to examine effects of intranasal dexmedetomidine, an α2-adrenorecptor agonist, on pain control and agitation in children undergoing BMT.

Primary Outcome

Pain greater than a zero reported in the Post Anesthesia Care Unit (PACU)

Interventions

  • DRUG Saline
  • DRUG Dexmedetomidine
  • DRUG Fentanyl

Trial Details

FieldValue
Enrollment Target 101 participants
Start Date 2005-08
Est. Completion 2008-12
Phase Phase 4

What the finished NCT00654329 record still lists

NCT00654329 is an interventional study that assigns participants to a tested intervention. The registered 101 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (81% lower).

The record links to 0 conditions, and to 3 interventions - of which Saline is the first listed.

NCT00654329 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00654329 about?

NCT00654329 is a clinical study titled "Dexmedetomidine vs Fentanyl for BMT". A randomized controlled clinical trial to examine effects of intranasal dexmedetomidine, an α2-adrenorecptor agonist, on pain control and agitation in children undergoing BMT.

What is the current status of trial NCT00654329?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 101 participants. The study started on 2005-08. Estimated completion is 2008-12.

What interventions are being tested in trial NCT00654329?

The interventions under investigation include: Saline (DRUG), Dexmedetomidine (DRUG), Fentanyl (DRUG).

Who is sponsoring clinical trial NCT00654329?

This trial is sponsored by Children's National Research Institute, which has 92 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00654329's enrollment target sits among peer trials

101 766th of 2000 higher than 1,231 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT04033497 · 101 participants · NA

    Treatment Response Assessment Maps to Delineate Necrosis From Tumor After Stereotactic Radiation in Brain Metastases

  • NCT05111574 · 101 participants · Phase 2

    Using Nivolumab Alone or With Cabozantinib to Prevent Mucosal Melanoma Return After Surgery

  • NCT05984680 · 101 participants

    COPD Care Pathway Among Patients With Cancer

  • NCT06266299 · 101 participants · Phase 1

    A Study of KK2269 in Adult Participants With Solid Tumors

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00654329, the US trial registry maintained by the National Library of Medicine. NCT00654329 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.