Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02595996 · ClinicalTrials.gov registry record · Phase 2

Propranolol Dose Escalation in Lymphedema in Patients

A Phase 2 study, sponsored by Columbia University.

Terminated
Registry status
Phase 2
Development phase
1
Enrollment target

NCT02595996 is a Phase 2 study that was terminated before completion, run by Columbia University. The registered enrollment target is 1 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02595996, a Phase 2 study, was terminated before completion, sponsored by Columbia University.

TERMINATED
Registry status
Phase 2
Development phase
1 participants
Enrollment target

Study Summary

This is a study to investigate the safety and efficacy of propranolol in the treatment of patients with primary lymphedema. The primary goal is to assess patient tolerability of increasing doses of propranolol. The secondary goal is to assess lymphedema symptoms and signs in response to propranolol treatment.

Interventions

  • DRUG Propranolol

Trial Details

FieldValue
Enrollment Target 1 participants
Start Date 2017-06-07
Est. Completion 2020-10-08
Phase Phase 2

Sponsor

Columbia University

958 total trials

What the Registry Record Tells You About NCT02595996

The ClinicalTrials.gov registry entry for NCT02595996 describes a study currently listed as terminated, categorized as Phase 2. The registered enrollment target is 1 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Columbia University, which has 958 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Propranolol is the first listed.

NCT02595996 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02595996 about?

NCT02595996 is a clinical study titled "Propranolol Dose Escalation in Lymphedema in Patients". This is a study to investigate the safety and efficacy of propranolol in the treatment of patients with primary lymphedema. The primary goal is to assess patient tolerability of increasing doses of propranolol. The secondary goal is to assess lymphedema symptoms and signs in response to propranolol ...

What is the current status of trial NCT02595996?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 1 participants. The study started on 2017-06-07. Estimated completion is 2020-10-08.

What interventions are being tested in trial NCT02595996?

The interventions under investigation include: Propranolol (DRUG).

Who is sponsoring clinical trial NCT02595996?

This trial is sponsored by Columbia University, which has 958 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.