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NCT01800682 · ClinicalTrials.gov registry record · Phase 1

A Pharmacokinetic Study to Evaluate the Dose-Proportionality of Tramadol (ULTRAM) Extended-Release (ER) in Healthy Participants

A Phase 1 study, sponsored by Janssen Research & Development.

Completed
Registry status
Phase 1
Development phase
30
Enrollment target

NCT01800682: Completed Phase 1 study, sponsored by Janssen Research & Development.

NCT01800682 is a Phase 1 study that has completed, run by Janssen Research & Development. The registered enrollment target is 30 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (50% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01800682, a Phase 1 study, has completed, sponsored by Janssen Research & Development.

COMPLETED
Registry status
Phase 1
Development phase
30 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the dose proportionality of the pharmacokinetics (explores what the body does to the drug) of tramadol in healthy adult participants.

Primary Outcome

The Cmax is the maximum plasma concentration.

Interventions

  • DRUG Tramodol Extended-Release (ER)

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2011-07
Est. Completion 2011-09
Phase Phase 1
Janssen Research & Development

593 total trials

What the finished NCT01800682 record still lists

NCT01800682 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (50% lower).

The record links to 0 conditions, and to 1 intervention - of which Tramodol Extended-Release (ER) is the first listed.

NCT01800682 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01800682 about?

NCT01800682 is a clinical study titled "A Pharmacokinetic Study to Evaluate the Dose-Proportionality of Tramadol (ULTRAM) Extended-Release (ER) in Healthy Participants". The purpose of this study is to evaluate the dose proportionality of the pharmacokinetics (explores what the body does to the drug) of tramadol in healthy adult participants.

What is the current status of trial NCT01800682?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 30 participants. The study started on 2011-07. Estimated completion is 2011-09.

What interventions are being tested in trial NCT01800682?

The interventions under investigation include: Tramodol Extended-Release (ER) (DRUG).

Who is sponsoring clinical trial NCT01800682?

This trial is sponsored by Janssen Research & Development, which has 593 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01800682's enrollment target sits among peer trials

30 1332nd of 2000 higher than 561 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 NCT01800682, the US trial registry maintained by the National Library of Medicine. NCT01800682 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.