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

NCT00732901 · ClinicalTrials.gov registry record · Phase 2

Clinical Neurobiology of Serotonin and Addiction

A Phase 2 study, sponsored by Virginia Commonwealth University.

Completed
Registry status
Phase 2
Development phase
160
Enrollment target

NCT00732901: Completed Phase 2 study, sponsored by Virginia Commonwealth University.

NCT00732901 is a Phase 2 study that has completed, run by Virginia Commonwealth University. The registered enrollment target is 160 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (20% higher). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00732901, a Phase 2 study, has completed, sponsored by Virginia Commonwealth University.

COMPLETED
Registry status
Phase 2
Development phase
160 participants
Enrollment target

Study Summary

The purpose of this study is to examine the relationship between 5-HT2R function, impulsivity and cue reactivity in cocaine dependent subjects and healthy controls and examine specific effects of escitalopram and mirtazapine on impulsivity and cue reactivity in human cocaine users.

Primary Outcome

The IMT was used to measure impulsivity. The IMT is a continuous performance test. Subjects were instructed to respond on the computer's left mouse button when a five-digit number the target stimulus appeared that was exactly like the preceding stimulus. A catch stimulus was a number that differed only slightly from the preceding number. Only one of the five digits was changed its position and value was determined randomly. Responses errors made to catch stimuli were considered commission errors

Interventions

  • DRUG Placebo
  • DRUG Escitalopram

Trial Details

FieldValue
Enrollment Target 160 participants
Start Date 2008-06
Est. Completion 2013-02
Phase Phase 2
Virginia Commonwealth University

558 total trials

What the finished NCT00732901 record still lists

NCT00732901 is an interventional study that assigns participants to a tested intervention. The registered 160 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (20% higher).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT00732901 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00732901 about?

NCT00732901 is a clinical study titled "Clinical Neurobiology of Serotonin and Addiction". The purpose of this study is to examine the relationship between 5-HT2R function, impulsivity and cue reactivity in cocaine dependent subjects and healthy controls and examine specific effects of escitalopram and mirtazapine on impulsivity and cue reactivity in human cocaine users.

What is the current status of trial NCT00732901?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 160 participants. The study started on 2008-06. Estimated completion is 2013-02.

What interventions are being tested in trial NCT00732901?

The interventions under investigation include: Placebo (DRUG), Escitalopram (DRUG).

Who is sponsoring clinical trial NCT00732901?

This trial is sponsored by Virginia Commonwealth University, which has 558 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00732901's enrollment target sits among peer trials

160 422nd of 2000 higher than 1,559 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

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

  • NCT00501826 · 160 participants · Phase 2

    Combination Chemotherapy and Nelarabine in Treating Patients With T-cell Acute Lymphoblastic Leukemia or Lymphoblastic Lymphoma

  • NCT00932139 · 160 participants · NA

    Effect of Electro-Acupuncture on Blood Pressure

  • NCT00992901 · 160 participants · Early Phase 1

    Role of Neural and Hormonal Regulation Factors on Insulin Secretion After Gastric Bypass Surgery

  • NCT01515527 · 160 participants · Phase 2

    Cladribine Plus Low Dose Cytarabine (LDAC) Alternating With Decitabine in Patients With Acute Myeloid Leukemia (AML) or High-Risk Myelodysplastic Syndrome (MDS)

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 NCT00732901, the US trial registry maintained by the National Library of Medicine. NCT00732901 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.