Lumbrokinase for Long Covid, Lyme, or Chronic Fatigue

Lumbrokinase for Adults With Long Covid, Post-treatment Lyme Disease Syndrome, and Myalgic Encephalomyelitis/Chronic Fatigue Syndrome

Recruiting Phase 1 Phase 2 Interventional Study
Long Covid Post-treatment Lyme Disease Syndrome Chronic Fatigue Syndrome Myalgic Encephalomyelitis
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 1/2
Study type
Interventional
Purpose
Treatment
Participants needed
120 (estimated)
Sponsor
Icahn School of Medicine at Mount Sinai · Other
Who this trial is looking for

This trial is looking for adults with Long Covid, Post-treatment Lyme Disease Syndrome, or Myalgic Encephalomyelitis/Chronic Fatigue Syndrome. Participants will take Lumbrokinase and help researchers understand its effects.

Are You a Good Fit for This Trial?

You may be able to join if

  • I am 18 years or older.
  • I have been diagnosed with Long Covid, Post-treatment Lyme Disease Syndrome, or Myalgic Encephalomyelitis/Chronic Fatigue Syndrome.
  • I have had COVID-19 or Lyme disease in the past.
  • I have a quality of life score of 70 or lower.
  • I was generally healthy before my illness.

You may not be able to join if

  • I am currently taking blood-thinning medications.
  • I am pregnant or breastfeeding.
  • I have an allergy to earthworms.
  • I have a history of bleeding or clotting disorders.
  • I have an autoimmune condition.
  • I have surgery scheduled during or immediately after the trial.

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

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About This Trial

This will be a pilot multi-arm clinical trial investigating the feasibility of Lumbrokinase (LK) as an intervention in three clinical cohorts: * Long Covid (LC) * Post-treatment Lyme disease syndrome (PTLDS) * Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS)

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Any gender * Aged 18+ * Baseline EQ-VAS ≤70; EQ-VAS before the index infection ≥80 (this information is collected as part of the baseline survey). * Diagnosed with only one of the following conditions: * Long Covid * Documented clinical history of confirmed or suspected acute …
Contacts

David Putrino, PhD, PT

212-241-8454

CoreResearch@mountsinai.org

CONTACT

Mackenzie Doerstling, MPH

212-241-8454

CoreResearch@mountsinai.org

CONTACT