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

NCT01680172 · ClinicalTrials.gov registry record · Phase 2

Oral Ketamine in the Treatment of Depression and Anxiety in Patients With Cancer

A Phase 2 study, sponsored by Mayo Clinic.

Terminated
Registry status
Phase 2
Development phase
5
Enrollment target

NCT01680172: Clinical Trial Phase 2 study, sponsored by Mayo Clinic.

NCT01680172 is a Phase 2 study that was terminated before completion, run by Mayo Clinic. The registered enrollment target is 5 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist → Add completion date to calendar (.ics) →

The verdict

NCT01680172, a Phase 2 study, was terminated before completion, sponsored by Mayo Clinic.

TERMINATED
Registry status
Phase 2
Development phase
5 participants
Enrollment target

Study Summary

Depression is common in patients with cancer. Current medications for depression, while effective, take several weeks to take effect. Ketamine has emerged as a drug with promise for cancer patients. In two reported cases, a single dose of ketamine induced rapid and moderately sustained symptom reduction in depression and anxiety with no adverse side effects. Benefit was seen in as little as 1 hour and sustained up to 30 days. This study is a randomized, double-blind, placebo-controlled investigation testing whether a single dose of ketamine improves depression and anxiety relative to placebo in patients with cancer.

Primary Outcome

Hospital Anxiety and Depression Scale (HADS) is a fourteen item scale. Seven of the items relate to anxiety and seven relate to depression. Each item on the questionnaire is scored from 0-3 and this means that a person can score between 0 (no symptoms) and 21 (severe symptoms) for either anxiety or depression. Cut-offs for identifying psychiatric distress has been reported in the literature to be \>10 for anxiety and \>8 for depression.

Interventions

  • DRUG Placebo
  • DRUG Ketamine

Trial Details

FieldValue
Enrollment Target 5 participants
Start Date 2012-08
Est. Completion 2015-02
Phase Phase 2
Mayo Clinic

2,844 total trials

Why NCT01680172 stopped before completion

NCT01680172 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 5 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (96% lower).

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

NCT01680172 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01680172 about?

NCT01680172 is a clinical study titled "Oral Ketamine in the Treatment of Depression and Anxiety in Patients With Cancer". Depression is common in patients with cancer. Current medications for depression, while effective, take several weeks to take effect. Ketamine has emerged as a drug with promise for cancer patients. In two reported cases, a single dose of ketamine induced rapid and moderately sustained symptom reduc...

What is the current status of trial NCT01680172?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 5 participants. The study started on 2012-08. Estimated completion is 2015-02.

What interventions are being tested in trial NCT01680172?

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

Who is sponsoring clinical trial NCT01680172?

This trial is sponsored by Mayo Clinic, which has 2,844 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01680172's enrollment target sits among peer trials

5 2000th of 2000 the lowest 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 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 NCT01680172, the US trial registry maintained by the National Library of Medicine. NCT01680172 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.