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NCT00319319 · ClinicalTrials.gov registry record · Phase 2

Nicotinic Receptor Augmentation of SSRI Antidepressants

A Phase 2 study, sponsored by Yale University.

Completed
Registry status
Phase 2
Development phase
60
Enrollment target

NCT00319319: Completed Phase 2 study, sponsored by Yale University.

NCT00319319 is a Phase 2 study that has completed, run by Yale University. The registered enrollment target is 60 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (55% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00319319, a Phase 2 study, has completed, sponsored by Yale University.

COMPLETED
Registry status
Phase 2
Development phase
60 participants
Enrollment target

Study Summary

The purpose of this study is to determine whether the nicotinic receptor antagonist mecamylamine hydrochloride (Inversine) can augment SSRI-refractory major depression symptoms, quality of life and cigarette smoking outcomes. A total of n=60 SSRI-refractory patients who are on stable doses of an SSRI are being recruited into this 8-week double-blind, randomized, placebo-controlled trial.

Interventions

  • DRUG Mecamylamine hydrochloride (Inversine)

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2003-01
Est. Completion 2007-01
Phase Phase 2
Yale University

1,492 total trials

What the finished NCT00319319 record still lists

NCT00319319 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (55% lower).

The record links to 0 conditions, and to 1 intervention - of which Mecamylamine hydrochloride (Inversine) is the first listed.

NCT00319319 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00319319 about?

NCT00319319 is a clinical study titled "Nicotinic Receptor Augmentation of SSRI Antidepressants". The purpose of this study is to determine whether the nicotinic receptor antagonist mecamylamine hydrochloride (Inversine) can augment SSRI-refractory major depression symptoms, quality of life and cigarette smoking outcomes. A total of n=60 SSRI-refractory patients who are on stable doses of an SSR...

What is the current status of trial NCT00319319?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 60 participants. The study started on 2003-01. Estimated completion is 2007-01.

What interventions are being tested in trial NCT00319319?

The interventions under investigation include: Mecamylamine hydrochloride (Inversine) (DRUG).

Who is sponsoring clinical trial NCT00319319?

This trial is sponsored by Yale University, which has 1,492 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00319319's enrollment target sits among peer trials

60 1027th of 2000 higher than 868 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT00319319, the US trial registry maintained by the National Library of Medicine. NCT00319319 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.