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Recruiting NCT07419360

NCT07419360 DRAIN: DRainage in Acute Decompensated Heart faIlure With Pleural effusioNs

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Clinical Trial Summary
NCT ID NCT07419360
Status Recruiting
Phase
Sponsor Albany Medical College
Condition Congestive Heart Failure(CHF)
Study Type INTERVENTIONAL
Enrollment 216 participants
Start Date 2026-02-15
Primary Completion 2029-02

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Thoracentesis

Eligibility Fast-Check

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What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 216 participants in total. It began in 2026-02-15 with a primary completion date of 2029-02.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The goal of this study is to assess if removal of fluid around the lungs (pleural effusion) by a routine procedure called as thoracentesis is helpful to decrease shortness of breath in hospitalized patients with congestive heart failure and have pleural effusion. Researchers will compare thoracentesis with medical therapy to medical therapy alone to see if one treatment is superior to the other treatment in relieving shortness of breath. Participants will : 1. Receive medical therapy with or without thoracentesis 2. Record degree of shortness of breath and quality of life before and after the intervention using predefined standard scales. 3. Telephonic call for 15- 30 mins at day 14 and 30 after enrollment to assess shortness of breath and quality of life

Eligibility Criteria

Inclusion Criteria: * Adult patients age \>18 years and. * Clinical diagnosis of acute decompensated heart failure with at least one clinical sign of volume overload (e.g., peripheral edema, pleural effusion, or ascites) and * Assessment of left ventricular ejection fraction (LVEF) by echocardiography performed during the time of index hospitalization or within 3 months prior to enrollment and * Serum NT-proBNP level of \>1000 pg/ml or Serum BNP\>250 pg/ml at the time of enrollment and * Radiographic evidence of moderate to large pleural effusion, defined as pleural fluid occupying more than 1/3rd of the hemithorax on chest X-ray. Exclusion Criteria: * Clinical indication for diagnostic thoracentesis - Presence of fever, clinical signs of infection, or atypical pleural effusion for CHF (unilateral left-sided effusion, findings suggestive of malignancy, infection, or alternative etiologies) or. * Loculated pleural effusion - Evidence of loculated pleural effusion on thoracic ultrasound, as defined as the presence of septations or complex homogenous echogenic fluid (see Imaging Assessment section) or. * Clinical indication for therapeutic thoracentesis - Presence of massive pleural effusion with acute respiratory failure requiring positive pressure ventilation, high-flow oxygen therapy (\>15 liters per minute of flow), or tension hydrothorax (massive effusion with mediastinal shift and hemodynamic compromise) or. * Contraindication to thoracentesis, uncontrolled bleeding diathesis, or irreversible INR \> 2.0 and platelet count \<50,000 or. * Patient with mechanical mitral valve, where anticoagulation cannot be safely held or. * Pleural procedure, such as but not limited to thoracentesis, chest tube placement, or thoracoscopy, within 3 months prior to enrollment or. * Cardiac or thoracic surgery within 3 months prior to enrollment or. * Requirement for chronic renal replacement therapy, such as hemodialysis or peritoneal dialysis or. * Pregnancy or * Inability or unwillingness to provide informed consent, or current incarceration (prisoners).

Contact & Investigator

Central Contact

Amit Chopra, MD

✉ chopraa1@amc.edu

📞 646-266-9476

Frequently Asked Questions

Who can join the NCT07419360 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Congestive Heart Failure(CHF). Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07419360 currently recruiting?

Yes, NCT07419360 is actively recruiting participants. Contact the research team at chopraa1@amc.edu for enrollment information.

Where is the NCT07419360 trial being conducted?

This trial is being conducted at Albany, United States.

Who is sponsoring the NCT07419360 clinical trial?

NCT07419360 is sponsored by Albany Medical College. The trial plans to enroll 216 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology