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Clinical Trials/NCT06833320
NCT06833320
Recruiting
Phase 1

A Double-blind, Prospective, Randomized Trial of Propranolol for the Treatment of Postoperative Chylothorax After Open Cardiac Surgery

June Wu1 site in 1 country50 target enrollmentStarted: September 9, 2025Last updated:

Overview

Phase
Phase 1
Status
Recruiting
Sponsor
June Wu
Enrollment
50
Locations
1
Primary Endpoint
Daily heart rates recorded in flow chart and 1 hour after each dose

Overview

Brief Summary

Postoperative chylothorax is a serious complication after open heart surgery for pediatric patients with congenital heart disease (CHD). While it was thought to be mechanical injury to the thoracic duct, recent research demonstrated that there are intrinsically abnormal lung lymphatics in CHD patients, and after open heart surgery, the fluid shifts that occur overwhelms these abnormal lung lymphatics. As a result, postoperative chylothorax occurs. Propranolol has been found to be helpful in resolving postoperative chylothorax very quickly (9 days) in a subset of postoperative chylothorax patients (60%). However, it is not known why some patients respond and some do not. The investigators hypothesize that propranolol is safe to use in this patient population, and that certain clinical factors will predict propranolol response, but more importantly, some clinical factors can be optimize to allow more patients with postoperative chylothorax to respond to and benefit from propranolol. In order to improve the understanding of how propranolol works and to maximize benefit to patients, the investigators propose to perform a prospective, randomized, double-blind clinical trial to learn how to best use propranolol in patients with postoperative chylothorax.

Detailed Description

This clinical trial will prospectively enroll eligible patients and randomize them to placebo or propranolol (1:1). This study will aim to enroll 50 patients, randomized to 25 placebo and 25 propranolol treatment. After patients have been consented, registered, and screened, they will be entered into the study. Participants will be randomized to placebo or propranolol in a 1:1 ratio. Randomization will be double-blinded, and each enrolled participant will be given a number and receive coded medication from the research pharmacy. Patients may undergo a screening MR lymphangiogram (MRL) prior to starting treatment. The criteria for an MRL will require that no additional sedation be given, and patient or parent/legal guardian consents to an MRL. Thus, only patients who are already sedated, or who will be able to undergo the MRL without sedation, and who opts in to the MRL will be eligible. Propranolol or placebo will be administered for 9 days after reaching the lowest effective goal dose not to exceed 2mg/kg/day, or maximum tolerated dose, after which the study groups will be unmasked.

Participants who have ≥80% reduction in volume of chylothorax drainage after 9 days of treatment and who received propranolol are identified as "responders". They will be taken off the study officially at this point as no more study interventions will be given. They will be tapered off of propranolol gradually as clinically indicated.

Participants who have ≥80% reduction in volume of chylothorax drainage but who received placebo will be the "natural history cohort". This will serve to demonstrate, as baseline, the percentage of participants who naturally resolve their chylothorax without intervention.

Patients who have <80% reduction in chylothorax drainage and who received propranolol, will be categorized as initial "non-responders". They will be officially taken off the study.

Participants who have <80% reduction in chylothorax drainage and who received placebo are considered a control group. They will be given propranolol for 9 days as a single-arm, open study and re-evaluated after a 9-day treatment. After 9 days at goal dosing, they will receive the same treatment as the responders and non-responders in the propranolol-treated group.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Investigator)

Eligibility Criteria

Ages
7 Days to 18 Years (Child, Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • ≥7 days and ≤18 years old at time of original cardiac surgery
  • Congenital structural cardiac anomaly necessitating surgical correction. Examples include but are not limited to: ASD, VSD, single ventricles, HLHS, Tetralogy of Fallot, transposition of great vessels, AV canal, heart transplant
  • developed high output postoperative chylothorax (≥10mL/kg/day), or
  • persistent chylous drainage at any volume for ≥7 days after open heart surgery for a congenital cardiac defect
  • ≥70% lymphocytes, or
  • pleural triglyeride (TG) ≥ half of serum TG, or chylomicron positive
  • for patients with lower than normal serum lymphocyte count (agedependent), ≥60% lymphocytes in pleural fluids
  • Must have measurable output (chylothorax output in mL)
  • Any level of respiratory support (room air, supplemental oxygen, CPAP/BIPAP, ventilatory support)
  • Any level of inpatient support (ICUs, step-down units, floor)

Exclusion Criteria

  • Pregnancy
  • Renal failure at time of enrollment
  • Hypotension despite pressor support
  • Unstable bradycardia without capacity for pacing
  • History of asthma or chronic bronchodilator therapy
  • Uncontrolled hypoglycemia or hyperglycemia as per investigators' judgment
  • Study participant will be removed from study if they failed 2 consecutive attempts to initiate propranolol (\>10% drop in BP/HR from age-adjusted normative range)
  • Study participant experiences ≥ Grade 3 AE (SAE)

Arms & Interventions

Placebo

Placebo Comparator

Placebo suspension will only have Ora-Blend

Intervention: Placebo (Drug)

Propranolol hydrochloride

Active Comparator

Subjects will be randomized to receive 2mg/kg/day. Propranolol will be administered orally, either as a tablet or as a solution, in equal divided doses three times a day.

Intervention: Propranolol Hydrochloride (Drug)

Outcomes

Primary Outcomes

Daily heart rates recorded in flow chart and 1 hour after each dose

Time Frame: 24 days

Safety outcome

Daily glucose levels

Time Frame: 24 days

Safety outcome

Daily blood pressures recorded in flow chart and 1 hour after each dose

Time Frame: 24 days

Safety outcome

Days with documented chest tube (# days), CXR

Time Frame: 24 days

Will also measure the daily output (volume) in the chest tube(s)

Initial volume of fluid drained (mL, mL/kg/day)

Time Frame: Day 0

The volume at the initial day of postoperative chylothorax diagnosis

Days hospitalized

Time Frame: 6 months

The length of hospital stay, from post-surgery to discharge

Expected and unexpected AEs, per patient

Time Frame: 24 days

Safety outcome

Secondary Outcomes

  • Thyroglobulin (TG) lymphocyte count(24 days)
  • Pre-operative and post-operative echocardiogram anatomic findings for patients with 4-chamber hearts(Pre-operative and up to 24 days)
  • Pre-operative and post-operative echocardiogram anatomic findings for patients with single ventricle (SV) physiology(Pre-operative and up to 24 days)
  • Percent of patients with Type 1 anatomy(Day 0)
  • Percent of patients with Type 2 anatomy(Day 0)
  • Percent of patients with Type 3 anatomy(Day 0)
  • Percent of patients with Type 4 anatomy(Day 0)
  • Serum albumin(24 days)
  • White Blood Cell (WBC) count(24 days)
  • C-Reactive Protein (CRP)(24 days)
  • Immunoglobulin level(24 days)
  • AT3 titer(24 days)
  • Protein S titer(24 days)
  • Protein C titer(24 days)
  • Hours on bypass during CHD surgery(During surgery)
  • Triglyceride level in chylothorax fluid(24 days)

Investigators

Sponsor
June Wu
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

June Wu

Associate Professor of Surgery

Columbia University

Study Sites (1)

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