RECRUITING

Pleuroscopy First Versus Thoracentesis First in Patients with Suspected Malignant Pleural Effusions

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This is a randomized control trial of patients with suspected malignant pleural effusions to compare whether patients who have a thoracentesis or pleuroscopy (pleural biopsy) obtain an adequate biopsy, achieve a diagnosis, and begin cancer-directed therapy faster.

Official Title

Pleuroscopy First Versus Thoracentesis First in Patients with Suspected Malignant Pleural Effusions

Quick Facts

Study Start:2025-03
Study Completion:2026-09-17
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06892691

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Referral for diagnostic pleural procedure.
  2. * Age ≥ 18 years.
  3. * Suspected malignant pleural effusion (Suggestive radiologic appearance (based on computed tomography or positron emission tomography) OR suspected cancer with associated effusion.)
  1. * Inability to provide informed consent.
  2. * Needs emergent drainage.
  3. * Pleural effusion is known to be malignant.
  4. * Suspected transudative, infectious or inflammatory effusion etiology.
  5. * Having prior inconclusive/non-diagnostic thoracentesis or pleuroscopy.
  6. * Patient is deemed by the clinical team to be more appropriate for VATS biopsy.
  7. * Terminally ill patients in whom a diagnosis will not change management, or who is unlikely to be a candidate for oncological treatment due to significant comorbidities.
  8. * Pregnancy

Contacts and Locations

Study Contact

Udit Chaddha, MBBS
CONTACT
212-241-5900
udit.chaddha@mssm.edu

Principal Investigator

Udit Chaddha, MBBS
PRINCIPAL_INVESTIGATOR
MOUNT SINAI HOSPITAL

Study Locations (Sites)

Mount Sinai West
New York, New York, 10019
United States
Mount Sinai Hospital
New York, New York, 10029
United States

Collaborators and Investigators

Sponsor: Icahn School of Medicine at Mount Sinai

  • Udit Chaddha, MBBS, PRINCIPAL_INVESTIGATOR, MOUNT SINAI HOSPITAL

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-03
Study Completion Date2026-09-17

Study Record Updates

Study Start Date2025-03
Study Completion Date2026-09-17

Terms related to this study

Additional Relevant MeSH Terms

  • Pleural Effusion
  • Cancer