Recruiting

Non-invasive Ventilation

Sponsor:

M.D. Anderson Cancer Center

Code:

NCT02464696

Conditions

Hematopoietic and Lymphoid Cell Neoplasm

Malignant Solid Neoplasm

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Methylprednisolone

Oxygen Therapy

Positive Air Pressure Device

Study Details

Brief 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.

Conditions

Hematopoietic and Lymphoid Cell Neoplasm

Malignant Solid Neoplasm

Study ID

NCT02464696

Start date

Oct 6, 2015

Status verified date

Mar, 2026

Completion date

Oct 1, 2026

Anticipated

Primary completion date

Oct 1, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Partial pressure of arterial oxygen (PaO2):fraction of inspired oxygen (FiO2) ratio =< 300 mmHg OR a peripheral capillary oxygen saturation (SaO2):FiO2 =< 357
  • Have a diagnosed malignancy
  • Chest radiograph or computed tomography (CT) scan within =< 3 months prior to study enrollment rules out primary or metastatic malignancy in the lungs or pleural space as a significant cause of respiratory insufficiency
  • Probability of survival is at least 6 months

Exclusion Criteria:

  • Presence of do not resuscitate (DNR)/do not intubate (DNI) orders at study entry
  • Clinical evidence of left heart failure as the main etiology for respiratory compromise
  • Evidence of active intrathoracic malignancy (primary or metastatic) in the lungs or pleural space that is a significant cause of respiratory insufficiency
  • Patients with acute chronic obstructive disease exacerbation as the primary etiology for respiratory failure
  • Evidence of accessory respiratory muscle use with breathing
  • Shock (need for vasopressor therapy or mean arterial pressure \[MAP\] < 60 despite fluid administration)
  • Oliguric acute renal failure (urine output < 500 ml/day) unless already on hemodialysis
  • Patient already on NIPPV at the time of screening
  • pH < 7.30 or partial pressure of carbon dioxide (pCO2) > 50 (if available)
  • Fixed upper airway obstruction
  • Airway or facial trauma that would hinder the use of a NIPPV mask
  • Uncontrolled tachy or bradyarrhythmia or active myocardial ischemia defined as either: atrial fibrillation with rapid ventricular response (heart rate \[HR\] > 120 beats per minute \[bpm\]), ventricular tachycardia or nonsustained ventricular tachycardia (any rate), supraventricular tachycardia (any rate), third degree heart block (any rate), heart rate less than 40 beats per minute (regardless of the rhythm)
  • Active myocardial ischemia defined as a clinical presentation at the time of screening consistent with acute coronary syndrome which includes unstable angina and electrocardiogram (EKG) changes suggestive of an either an acute ST elevation myocardial infarction (new ST elevations or new left bundle branch block) or acute non-ST elevation myocardial infarction (new ST depressions, new T wave inversions)
  • Glasgow Coma Scale (GCS) < 8 or inadequate airway protective reflexes
  • Undrained pneumothorax/pneumomediastinum
  • Copious secretions (> 20 cc's of sputum production per hour or significant hemoptysis defined as > 100 cc's of hemoptysis in a 24 hour period
  • Risk for gastric aspiration (ie; ileus, esophageal or bowel obstruction, active vomiting)
  • Recent esophageal, gastric or bowel surgery (within 3 weeks of study enrollment)
  • Inability to cooperate with NIPPV
  • Refusal to receive NIPPV
  • Respiratory arrest

Study Design

Enrollment

256 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Supportive Care

Interventions and Outcome Measures

Arms

experimental: Arm A (NIPPV therapy)

Patients undergo intermittent NIPPV, with the recommended schedule comprising 2 hours on NIPPV followed by =< 2 hours off NIPPV and continuous NIPPV at night or while sleeping for 8 hours per day, for 28 days or until discharged from the hospital.

active comparator: Arm B (high flow oxygen therapy)

Patients continue to receive high flow nasal cannula oxygen therapy using current protocol for titration of high flow oxygen therapy for 28 days or until discharged from the hospital. Patients may receive NIPPV if they develop evidence of accessory muscle use with breathing or at the discretion of the treating physician.

Interventions

Methylprednisolone

IPS cohort only

Oxygen Therapy

Receive high flow oxygen therapy

Positive Air Pressure Device

Undergo NIPPV

Primary outcome measure

  • Percent of patients who require intubation or meet criteria for intubation [ Time Frame: Up to 28 days from study inclusion ]

Central Contacts and Locations

Central contacts

Nisha Rathi, MD

713-792-5040NRathi@mdanderson.org

Locations

M D Anderson Cancer Center

Recruiting

Houston, Texas, United States, 77030

Contacts

Nisha Rathi

713-792-5040NRathi@mdanderson.org

Principal Investigator:

Nisha Rathi

More Information

Sponsor

M.D. Anderson Cancer Center

Last update posted

Mar 5, 2026

Last verified

Mar, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-08. This information was provided to ClinicalTrials.gov by M.D. Anderson Cancer Center on 2026-03-05.