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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT03953261
Other study ID # 5190041
Secondary ID
Status Terminated
Phase Phase 2
First received
Last updated
Start date September 1, 2019
Est. completion date April 13, 2022

Study information

Verified date August 2022
Source Loma Linda University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this investigator initiated study is to determine the efficacy of curcumin on disease activity of subjects with systemic lupus erythematous. Curcumin has been found to have anti-inflammatory effects and has been found to improve disease activity in lupus patients. In addition, subjects with rheumatoid arthritis as well as osteoarthritis have also found benefit for their disease activity.


Recruitment information / eligibility

Status Terminated
Enrollment 23
Est. completion date April 13, 2022
Est. primary completion date April 13, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Provision of signed and dated informed consent form - Stated willingness to comply with all study procedures and availability for the duration of the study - Male or female, aged 18 or older - Diagnosed with Systemic Lupus Erythematous according to the 2012 Systemic Lupus International Collaborating Clinics Classification Criteria. - SLEDAI score of 6 or higher - Ability to take oral medication and be willing to adhere to the study drug regimen Exclusion Criteria: - Inability to provide written consent for study participation - Use of curcumin supplements within 30 days of enrollment of study - Liver function disorders (AST/ALT > 2.5x upper limit of normal) - Pregnancy or lactation - Known allergic reactions to turmeric - Subjects who are admitted for recent hospitalization within past 60 days - Treatment with another investigational drug or other intervention within past 60 days - Subjects with end stage renal disease on dialysis - Subjects who lack the ability to provide consent

Study Design


Intervention

Drug:
Curcumin supplement
Intervention is 2 grams of curcumin supplement per day

Locations

Country Name City State
United States Loma Linda University Loma Linda California

Sponsors (1)

Lead Sponsor Collaborator
Loma Linda University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in SLEDAI Number of participants with change in SLEDAI by 2 points by Day 90 90 days
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