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NCT00685295 · ClinicalTrials.gov registry record · Phase 1

Fentanyl Administered Intraorally for Rapid Treatment of Orthopedic Pain

A Phase 1 study of Pain, Fracture, Sprain, sponsored by Massachusetts General Hospital.

Completed
Registry status
Phase 1
Development phase
60
Enrollment target
1
Study location

NCT00685295: Completed Phase 1 study of Pain, Fracture, Sprain, sponsored by Massachusetts General Hospital.

NCT00685295 is a Phase 1 study of Pain, Fracture, Sprain that has completed, run by Massachusetts General Hospital. The registered enrollment target is 60 participants, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target. The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00685295, a Phase 1 study of Pain, Fracture, Sprain, has completed, sponsored by Massachusetts General Hospital.

COMPLETED
Registry status
Phase 1
Development phase
60 participants
Enrollment target
1
Study location

Study Summary

Assess whether transbuccal fentanyl provides more rapid relief of orthopedic pain, than does the comparator Percocet

Primary Outcome

Time it took for subjects to achieve a pain score reduction of 2 units (on a 0 to 10 scale)

Conditions Studied

Interventions

  • DRUG Oxycodone
  • DRUG Fentanyl
  • DRUG Lansoprazole

Study Locations (1)

Massachusetts

  • Massachusetts General Hospital - Boston

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2008-08
Est. Completion 2009-02
Phase Phase 1
Massachusetts General Hospital

2,032 total trials

What the finished NCT00685295 record still lists

NCT00685295 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target.

The record links to 1 condition, with Pain, Fracture, Sprain appearing as the primary indexed condition, and to 3 interventions - of which Oxycodone is the first listed.

NCT00685295 reports a single indexed study location in Massachusetts.

Frequently Asked Questions

What is clinical trial NCT00685295 about?

NCT00685295 is a clinical study titled "Fentanyl Administered Intraorally for Rapid Treatment of Orthopedic Pain". Assess whether transbuccal fentanyl provides more rapid relief of orthopedic pain, than does the comparator Percocet

What is the current status of trial NCT00685295?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 60 participants. The study started on 2008-08. Estimated completion is 2009-02.

What conditions does trial NCT00685295 study?

This clinical trial studies the following conditions: Pain, Fracture, Sprain.

What interventions are being tested in trial NCT00685295?

The interventions under investigation include: Oxycodone (DRUG), Fentanyl (DRUG), Lansoprazole (DRUG).

Who is sponsoring clinical trial NCT00685295?

This trial is sponsored by Massachusetts General Hospital, which has 2,032 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00685295 being conducted?

This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

How this trial's enrollment target compares

Where NCT00685295's enrollment target sits among peer trials

60 831st of 2000 higher than 1,106 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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

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Source: ClinicalTrials.gov NCT00685295, the US trial registry maintained by the National Library of Medicine. NCT00685295 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.