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

NCT01842334 · ClinicalTrials.gov registry record · Phase 1

D-cycloserine (DCS) Pretreatment + CBT + Nicotine Replacement Therapy for Smoking Cessation (DCS)

A Phase 1 study, sponsored by Mclean Hospital.

Terminated
Registry status
Phase 1
Development phase
22
Enrollment target

NCT01842334: Clinical Trial Phase 1 study, sponsored by Mclean Hospital.

NCT01842334 is a Phase 1 study that was terminated before completion, run by Mclean Hospital. The registered enrollment target is 22 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (63% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01842334, a Phase 1 study, was terminated before completion, sponsored by Mclean Hospital.

TERMINATED
Registry status
Phase 1
Development phase
22 participants
Enrollment target

Study Summary

1. Compare the relative efficacy of ten weeks of once weekly 250 mg D-cycloserine (DCS) vs. placebo (both in conjunction with cognitive behavioral therapy (CBT) and nicotine replacement therapy (NRT) on reducing cigarette smoking in treatment-seeking nicotine-dependent outpatients. 2. Compare the relative efficacy of ten weeks of once weekly 250 mg DCS vs. placebo on the process of extinction and the memory encoding process.

Primary Outcome

Cigarette smoking at 10 weeks as measured by carbon monoxide levels and self-report measurements.

Interventions

  • BEHAVIORAL Cognitive Behavioral Therapy
  • DRUG Nicotine Replacement Therapy

Trial Details

FieldValue
Enrollment Target 22 participants
Start Date 2013-04
Est. Completion 2017-08
Phase Phase 1
Mclean Hospital

140 total trials

Why NCT01842334 stopped before completion

NCT01842334 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 22 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (63% lower).

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

NCT01842334 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01842334 about?

NCT01842334 is a clinical study titled "D-cycloserine (DCS) Pretreatment + CBT + Nicotine Replacement Therapy for Smoking Cessation (DCS)". 1. Compare the relative efficacy of ten weeks of once weekly 250 mg D-cycloserine (DCS) vs. placebo (both in conjunction with cognitive behavioral therapy (CBT) and nicotine replacement therapy (NRT) on reducing cigarette smoking in treatment-seeking nicotine-dependent outpatients. 2. Compare the re...

What is the current status of trial NCT01842334?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 22 participants. The study started on 2013-04. Estimated completion is 2017-08.

What interventions are being tested in trial NCT01842334?

The interventions under investigation include: Cognitive Behavioral Therapy (BEHAVIORAL), Nicotine Replacement Therapy (DRUG).

Who is sponsoring clinical trial NCT01842334?

This trial is sponsored by Mclean Hospital, which has 140 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01842334's enrollment target sits among peer trials

22 1601st of 2000 higher than 386 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

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

  • NCT02508038 · 22 participants · Phase 1

    Alpha/Beta CD19+ Depleted Haploidentical Transplantation + Zometa for Pediatric Hematologic Malignancies and Solid Tumors

  • NCT03099356 · 22 participants · Phase 2

    Cyclophosphamide and Sirolimus for the Treatment of Metastatic, RAI-refractory, Differentiated Thyroid Cancer

  • NCT03676647 · 22 participants

    Diagnostic DNA Methylation Signature in Diagnosing Thyroid Cancer After Fine-Needle Aspiration in Patients With Thyroid Nodules

  • NCT04569591 · 22 participants · NA

    DDAVP for Pituitary Adenoma

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 NCT01842334, the US trial registry maintained by the National Library of Medicine. NCT01842334 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.