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Effectiveness of Bronchoscopic Interventions for Malignant Airway Obstruction

M.D. Anderson Cancer Center logo

M.D. Anderson Cancer Center

Status

Completed

Conditions

Lung Cancer

Treatments

Behavioral: Medical Data Collection

Study type

Observational

Funder types

Other

Identifiers

NCT03326570
NCI-2018-01276 (Registry Identifier)
2011-0563

Details and patient eligibility

About

The goal of this clinical research study is learn about side effects and the success of bronchoscopies when performed in cancer patients with and without symptoms.

This is an investigational study.

Up to 110 patients will take part in this study. All will be enrolled at MD Anderson.

Full description

If participant agrees to take part in this study, researchers will collect information from participant's medical records.

Length of Study:

Researchers will continue to collect participant's medical information for up to 2 years.

Additional Information:

Participant's data will be kept in a database on a password-protected computer in a secure office. This information will only be available to the study doctors and staff.

Enrollment

110 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

° All patients undergoing interventional bronchoscopy during the first 12 months will be enrolled, with follow-up occurring out to 2 years from the study startup (the duration of the grant).

Exclusion criteria

  • Age less than 18 years,
  • Inability to participate in telephone follow-up

Trial design

110 participants in 1 patient group

Bronchoscopy Data Collection
Description:
Medical information collected after bronchoscopy for up to 2 years.
Treatment:
Behavioral: Medical Data Collection

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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