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

NCT00271596 · ClinicalTrials.gov registry record · Phase 2

Citalopram to Enhance Cognition in HD

A Phase 2 study, sponsored by University of Iowa.

Completed
Registry status
Phase 2
Development phase
33
Enrollment target

NCT00271596: Completed Phase 2 study, sponsored by University of Iowa.

NCT00271596 is a Phase 2 study that has completed, run by University of Iowa. The registered enrollment target is 33 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (75% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00271596, a Phase 2 study, has completed, sponsored by University of Iowa.

COMPLETED
Registry status
Phase 2
Development phase
33 participants
Enrollment target

Study Summary

This research plan proposes to conduct a double-blind, placebo-controlled pilot clinical trial in 36 adults with mild Huntington's disease (HD) to address the following research aims: 1. To determine the effect of citalopram compared to placebo in patients with early HD on executive function and other outcome variables including functional measures (health-related quality of life, work productivity, and self-reported attention), motor performance, and psychiatric status, 2. To study the relationship between executive function and functional status in patients with early HD after selective serotonin reuptake inhibitor (SSRI) treatment, and 3. To examine the effect of citalopram treatment on volumetric and metabolic (i.e, N-acetyl-aspartate concentration) measures in the neostriatum among patients with recently diagnosed Huntington's disease.

Primary Outcome

Full Scale Name: The Executive Composite Score (ECS). Definition: Subscales were averaged to compute this composite total score. The ECS is the weighted average of performance on 6 subtests of executive function, including (1) the Controlled Oral Word Association Test, (2) Symbol Digit Modalities test; (3) Stroop Color Word Test (Interference Trial), (4) Trail Making test (Part B), (5) Letter-Number Sequencing, and (6) Animal Naming. Construct Measured: Thinking tasks involving planning, working

Interventions

  • DRUG Placebo
  • DRUG 20mg daily citalopram

Trial Details

FieldValue
Enrollment Target 33 participants
Start Date 2005-11
Est. Completion 2011-11
Phase Phase 2
University of Iowa

228 total trials

What the finished NCT00271596 record still lists

NCT00271596 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 33 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (75% lower).

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

NCT00271596 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00271596 about?

NCT00271596 is a clinical study titled "Citalopram to Enhance Cognition in HD". This research plan proposes to conduct a double-blind, placebo-controlled pilot clinical trial in 36 adults with mild Huntington's disease (HD) to address the following research aims: 1. To determine the effect of citalopram compared to placebo in patients with early HD on executive function and ot...

What is the current status of trial NCT00271596?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 33 participants. The study started on 2005-11. Estimated completion is 2011-11.

What interventions are being tested in trial NCT00271596?

The interventions under investigation include: Placebo (DRUG), 20mg daily citalopram (DRUG).

Who is sponsoring clinical trial NCT00271596?

This trial is sponsored by University of Iowa, which has 228 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00271596's enrollment target sits among peer trials

33 1553rd of 2000 higher than 438 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

  • NCT02861898 · 33 participants · Phase 1

    Super-selective Intra-arterial Repeated Infusion of Cetuximab for the Treatment of Newly Diagnosed Glioblastoma

  • NCT04871607 · 33 participants · Phase 2

    Yttrium-90 Labeled Anti-CD25 Monoclonal Antibody Combined With BEAM Chemotherapy Conditioning for the Treatment of Primary Refractory or Relapsed Hodgkin Lymphoma

  • NCT05071937 · 33 participants · Phase 2

    ZEN003694 Combined With Talazoparib in Patients With Recurrent Ovarian Cancer

  • NCT05168618 · 33 participants · Phase 2

    Cabozantinib and Atezolizumab for the Treatment of Metastatic Castration-Resistant Prostate Cancer, The AtezoCab Trial

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 NCT00271596, the US trial registry maintained by the National Library of Medicine. NCT00271596 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.