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NCT02464696 · ClinicalTrials.gov registry record · NA

Non-invasive Ventilation in Reducing the Need for Intubation in Patients With Cancer and Respiratory Failure

A NA study of Malignant Solid Neoplasm and Hematopoietic and Lymphoid Cell Neoplasm, sponsored by M.D. Anderson Cancer Center.

Recruiting
Registry status
NA
Development phase
256
Enrollment target
1
Study location

NCT02464696: Recruiting NA study of Malignant Solid Neoplasm and Hematopoietic and Lymphoid Cell Neoplasm, sponsored by M.D. Anderson Cancer Center.

NCT02464696 is a NA study of Malignant Solid Neoplasm and Hematopoietic and Lymphoid Cell Neoplasm that is actively recruiting participants, run by M.D. Anderson Cancer Center. The registered enrollment target is 256 participants, below the 1,139-participant average among 176 other Malignant Solid Neoplasm trials with a reported enrollment target (78% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02464696, a NA study of Malignant Solid Neoplasm and Hematopoietic and Lymphoid Cell Neoplasm, is actively recruiting participants, sponsored by M.D. Anderson Cancer Center.

RECRUITING
Registry status
NA
Development phase
256 participants
Enrollment target
1
Study location

Study Summary

This randomized clinical trial studies how well non-invasive ventilation works in reducing the need for intubation, or placement of a tube in the windpipe, in patients with cancer and respiratory failure. Respiratory failure is a condition in which not enough oxygen passes from the lungs to the blood, and is a common cause of admission to the emergency room in patients with hematological and solid tumor patients. Non-invasive positive pressure ventilation (NIPPV) is a method of delivering oxygen using a mask. It is not yet known whether NIPPV is better at improving the amount of oxygen in the blood, reducing shortness of breath, and the need for intubation than standard high flow oxygen (a tube with 2 prongs placed in the nostrils) in patients with cancer and respiratory failure.

Primary Outcome

Fisher's exact test or a chi-squared test will be used to assess the association between two categorical variables. The intubation rate by 28 days and 95% confidence intervals will be estimated for each treatment arm. Logistic regression will be utilized to assess the effect of patient prognostic factors on the intubation rate by 28 days.

Interventions

  • PROCEDURE Oxygen Therapy
  • DRUG Methylprednisolone
  • DEVICE Positive Air Pressure Device

Study Locations (1)

Texas

  • M D Anderson Cancer Center - Houston

Trial Details

FieldValue
Enrollment Target 256 participants
Start Date 2015-10-06
Est. Completion 2026-10-01
Phase NA
M.D. Anderson Cancer Center

2,692 total trials

What NCT02464696 shows while recruiting

NCT02464696 is an interventional study that assigns participants to a tested intervention. The registered 256 participants enrollment target is mid-sized for trials with a published cap, below the 1,139-participant average among 176 other Malignant Solid Neoplasm trials with a reported enrollment target (78% lower).

The record links to 2 conditions, with Malignant Solid Neoplasm appearing as the primary indexed condition, and to 3 interventions - of which Oxygen Therapy is the first listed.

NCT02464696 reports a single indexed study location in Texas.

Frequently Asked Questions

What is clinical trial NCT02464696 about?

NCT02464696 is a clinical study titled "Non-invasive Ventilation in Reducing the Need for Intubation in Patients With Cancer and Respiratory Failure". This randomized clinical trial studies how well non-invasive ventilation works in reducing the need for intubation, or placement of a tube in the windpipe, in patients with cancer and respiratory failure. Respiratory failure is a condition in which not enough oxygen passes from the lungs to the bloo...

What is the current status of trial NCT02464696?

This trial is currently recruiting. It is a NA study. The enrollment target is 256 participants. The study started on 2015-10-06. Estimated completion is 2026-10-01.

What conditions does trial NCT02464696 study?

This clinical trial studies the following conditions: Malignant Solid Neoplasm, Hematopoietic and Lymphoid Cell Neoplasm.

What interventions are being tested in trial NCT02464696?

The interventions under investigation include: Oxygen Therapy (PROCEDURE), Methylprednisolone (DRUG), Positive Air Pressure Device (DEVICE).

Who is sponsoring clinical trial NCT02464696?

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

Where is trial NCT02464696 being conducted?

This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Malignant Solid Neoplasm

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT02464696's enrollment target sits among peer trials

256 53rd of 176 higher than 124 of 176 other Malignant Solid Neoplasm trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Malignant Solid Neoplasm 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 NCT02464696, the US trial registry maintained by the National Library of Medicine. NCT02464696 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.