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Antihistamine

Cromolyn Sodium for Chronic Prostatitis

Phase < 1
Waitlist Available
Led By Praveen Thumbikat, PhD
Research Sponsored by Northwestern University
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 3 weeks
Awards & highlights

Summary

This trial tests two medications, Cromolyn Sodium and Cetirizine, to help men with chronic prostatitis and chronic pelvic pain syndrome. These medications aim to reduce pain and swelling by stopping certain immune cells from releasing harmful chemicals. The study will measure changes in symptoms and specific chemical levels in the body over time.

Eligible Conditions
  • Chronic Prostatitis

Timeline

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

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Mast cell tryptase levels in expressed prostatic secretions
Secondary study objectives
AUA-SI score
NIH-CPSI score

Trial Design

1Treatment groups
Experimental Treatment
Group I: Treatment armExperimental Treatment2 Interventions
Treated arm with cromolyn sodium and cetirizine hydrochloride
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Cromoglicic acid
FDA approved
Cetirizine
FDA approved

Find a Location

Who is running the clinical trial?

Northwestern UniversityLead Sponsor
1,625 Previous Clinical Trials
937,269 Total Patients Enrolled
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)NIH
2,410 Previous Clinical Trials
4,324,871 Total Patients Enrolled
Praveen Thumbikat, PhDPrincipal Investigator - Northwestern University
Northwestern University
2 Previous Clinical Trials
197 Total Patients Enrolled
~2 spots leftby Sep 2025
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