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RecruitingPhase 2interventionalRules rewrite

Phase 2: Immunoadsorption for Long COVID

Some people continue to have serious symptoms long after COVID-19, such as extreme fatigue and feeling worse after activity. In some patients, this may happen because the immune system is attacking the body by mistake.

Official registry: https://clinicaltrials.gov/study/NCT07316127 · Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) · enrollment listed as 70

What this phase means

Phase 2: researchers already know a roughly safe dose (from phase 1). This stage asks whether the treatment actually helps the condition, and watches side effects more closely.

Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.

What the registry says happens

If you join, the listed intervention(s) are Immunoadsorption, or Sham Comparator. The registry lists allocation as randomized. Some people continue to have serious symptoms long after COVID-19, such as extreme fatigue and feeling worse after activity.

They plan to enroll about 70 people at Amsterdam. Taking part typically means using or being fitted with a device plus check-ins.

Official title (unrewritten)

A Placebo-Controlled, Double-Blind, Randomized Trial Phase I-II With Immunoadsorption in Autoimmune Long COVID

Interventions: Immunoadsorption, Sham Comparator

Primary outcome (registry wording): Change in fatigue measured by the Fatigue Assessment Scale (FAS)

Who it is for (from inclusion criteria)

  • Ages 18 Years to 65 Years
  • Long COVID based on the WHO-criteria
  • PEM according to the DSQ-PEM
  • BELL's functionality score 20-70%
  • Good health prior to the long COVID diagnosis (WHO performance score 0)

Public study contact (from the registry)

Daphne Schouten, MD

+31 20 566 9111

postcovidtrials@amsterdamumc.nl

Published on ClinicalTrials.gov. Contact them as a possible participant. They decide eligibility.

Sites listed on ClinicalTrials.gov

1 listed

Related recruiting trials in this snapshot

RecruitingNot a traditional drug phasePaiporta, Valencia
Not a traditional drug phase: Transcranial Direct Current Therapy (tDCS) for COVID-19

This study aims to verify the how well it works/effectiveness of treatment with transcranial direct current stimulation (TDCS) in patients with Long Covid who experience headaches, migraines, and chronic pain, such as arthralgia and myalgia, as well as sleep problems. Transcranial direct current stimulation is used in the field of Physiotherapy and Rehabilitation, with results that have proven to be effective for treating patients suffering from symptoms like migraines, headaches, chronic pain, fibromyalgia, or chronic neuropathic pain and insomnia.

NCT05780450 · Official ClinicalTrials.gov record · Fundación Universidad Católica de Valencia San Vicente Mártir

FAQ about this NCT record

Is NCT07316127 still recruiting?

The sponsor posted status “Recruiting” on ClinicalTrials.gov at last ingest. Sites can pause independently. Confirm with the official record and the listed contact.

What phase is NCT07316127?

Phase 2. Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.

Can PlainTrials tell me if I qualify for NCT07316127?

No. The inclusion and exclusion lists on this page are readable extracts of the public eligibility block. Only the study team can screen you.

How to read a ClinicalTrials.gov record · Questions to ask the coordinator · Glossary