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NCT01670097 · ClinicalTrials.gov registry record · Phase 2

Dexamethasone Dyspnea Study

A Phase 2 study, sponsored by M.D. Anderson Cancer Center.

Completed
Registry status
Phase 2
Development phase
52
Enrollment target

NCT01670097: Completed Phase 2 study, sponsored by M.D. Anderson Cancer Center.

NCT01670097 is a Phase 2 study that has completed, run by M.D. Anderson Cancer Center. The registered enrollment target is 52 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (61% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01670097, a Phase 2 study, has completed, sponsored by M.D. Anderson Cancer Center.

COMPLETED
Registry status
Phase 2
Development phase
52 participants
Enrollment target

Study Summary

The goal of this clinical research study is to learn if dexamethasone can help reduce shortness of breath in cancer patients. Researchers also want to learn if it can help to improve lung function and quality of life. In this study, dexamethasone will be compared to a placebo. Dexamethasone is commonly used for treatment of nausea, tiredness, and pain. It may help patients with shortness of breath. A placebo is not a drug. It looks like the study drug but is not designed to treat any disease or illness. It is designed to be compared with a study drug to learn if the study drug has any real effect.

Primary Outcome

Number of participants who completed the dyspnea numeric rating scale on Day 7

Interventions

  • DRUG Placebo
  • DRUG Dexamethasone
  • BEHAVIORAL Questionnaires
  • OTHER Phone Calls
  • DEVICE Spirometer

Trial Details

FieldValue
Enrollment Target 52 participants
Start Date 2013-01
Est. Completion 2021-01-26
Phase Phase 2
M.D. Anderson Cancer Center

2,692 total trials

What the finished NCT01670097 record still lists

NCT01670097 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 52 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (61% lower).

The record links to 0 conditions, and to 5 interventions - of which Placebo is the first listed.

NCT01670097 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01670097 about?

NCT01670097 is a clinical study titled "Dexamethasone Dyspnea Study". The goal of this clinical research study is to learn if dexamethasone can help reduce shortness of breath in cancer patients. Researchers also want to learn if it can help to improve lung function and quality of life. In this study, dexamethasone will be compared to a placebo. Dexamethasone is comm...

What is the current status of trial NCT01670097?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 52 participants. The study started on 2013-01. Estimated completion is 2021-01-26.

What interventions are being tested in trial NCT01670097?

The interventions under investigation include: Placebo (DRUG), Dexamethasone (DRUG), Questionnaires (BEHAVIORAL), Phone Calls (OTHER), Spirometer (DEVICE).

Who is sponsoring clinical trial NCT01670097?

This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01670097's enrollment target sits among peer trials

52 1181st of 2000 higher than 811 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 NCT01670097, the US trial registry maintained by the National Library of Medicine. NCT01670097 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.