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C1 esterase inhibitor

RUCONEST for Chronic Fatigue Syndrome

Phase 4
Waitlist Available
Research Sponsored by IMMUNOe Research Centers
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up week 17
Awards & highlights

Study Summary

This study is evaluating whether a drug may help improve neurological symptoms for individuals who have been infected with the SARS virus.

Eligible Conditions
  • Chronic Fatigue Syndrome
  • Coronavirus
  • Post-Viral Syndrome

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~week 17
This trial's timeline: 3 weeks for screening, Varies for treatment, and week 17 for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Immunological Biomarkers (Com)
Immunological Biomarkers (GAD)
Immunological Biomarkers (Ig)
+17 more

Trial Design

2Treatment groups
Active Control
Placebo Group
Group I: RUCONESTActive Control1 Intervention
IV Ruconest
Group II: PlaceboPlacebo Group1 Intervention
Placebo

Find a Location

Who is running the clinical trial?

IMMUNOe Research CentersLead Sponsor
3 Previous Clinical Trials
56 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Recent research and studies
clinicaltrials.govStudy
Study to Evaluate the Benefit of RUCONEST in Improving Neurological Symptoms in Post COVID-19 Infection
Isaac Melamed, MD 2020. "Study to Evaluate the Benefit of RUCONEST in Improving Neurological Symptoms in Post COVID-19 Infection". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT04705831.
~9 spots leftby Apr 2025
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