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Clinical Trials/KCT0002651
KCT0002651Recruiting未知

A randomized, double-blind, placebo-controlled trial of ramosetron in patients with fibromyalgia.

Chonnam National University Hospital0 sites80 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
未知
Status
Recruiting
Enrollment
80

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional Study

Eligibility Criteria

Ages
18(Year) to 80(Year) (—)
Sex
All

Inclusion Criteria

  • Patients between 18 and 80 years of age who meet the following criteria:
  • Disease: The definition of fibromyalgia is based on the criteria published by the American Society of Rheumatology (ACR) in 2010, and the patients who meet the following criteria are eligible.
  • 1) The patients who meet the 2010 ACR criteria for fibromyalgia
  • 2) No response after 4 weeks of standard medication
  • 3) Pain VAS 40 and FIQ score of 45 or more
  • 4) The patients who are fully informed about the study and signed the informed consent.

Exclusion Criteria

  • 1) Patients complaining of pain due to other rheumatic diseases.
  • 2) The patients who had a certain diseases such as uncontrolled tumors
  • 3) If patients have uncontrolled illness or psychiatric illness
  • 4) If patients have a history of drug addiction
  • 5) Patients who are pregnant or expect to become pregnant
  • 6) If there is a previous history of study drug use before 30 days
  • 7) Patients with severe complications due to drug allergy
  • are excluded from this study.

Investigators

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