Evaluating Effects of Curcumin in Moderate to Severe Asthmatics

Sponsor
Loma Linda University (Other)
Overall Status
Withdrawn
CT.gov ID
NCT04353310
Collaborator
(none)
0
2
2.3

Study Details

Study Description

Brief Summary

The purpose of this investigator-initiated study is to evaluate the effects of oral curcumin supplementation versus placebo in adult patients with moderate to severe asthma. Curcumin, a derivative of turmeric, has been shown in animal models to inhibit the secretion of pro-inflammatory cytokines and decrease airway constriction and hyperreactivity with only a few observational studies available in humans with discordant results.

Condition or Disease Intervention/Treatment Phase
Phase 2

Study Design

Study Type:
Interventional
Actual Enrollment :
0 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Care Provider, Investigator)
Primary Purpose:
Prevention
Official Title:
Evaluating the Effects of Curcumin in Moderate to Severe Asthmatics
Anticipated Study Start Date :
Sep 1, 2021
Actual Primary Completion Date :
Nov 9, 2021
Actual Study Completion Date :
Nov 9, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Curcumin

Drug: Curcumin
Curcumin 1500mg PO BID

Placebo Comparator: Placebo

Other: Placebo
identical in appearance to curcumin

Outcome Measures

Primary Outcome Measures

  1. Asthma Control [3 months]

    defined by the Asthma Control Test, which has a 5-point scale (for symptoms and activities: 1=all the time to 5= not at all; for asthma control rating: 1=not controlled at all to 5=completely controlled)

Secondary Outcome Measures

  1. Number of Severe Asthma Exacerbations in 3 Months [3 months]

  2. Cumulative Days Missed From School or Work in 3 Months [3 months]

  3. Spirometry [3 months]

    FEV1/FVC ratio, FEV1: forced expiratory volume in one second, FVC: forced vital capacity

  4. Exhaled nitric oxide [3 months]

  5. Total IgE [3 months]

  6. Total plasma eosinophil count [3 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Provision of signed and dated informed consent form

  2. Stated willingness to comply with all study procedures and availability for the duration of the study

  3. Male or female, aged 18 and older

  4. Physician diagnosed moderate to severe asthma: (GINA 2018)

  1. Stable asthma that requires ICS/LABA and/or an additional controller agent (i.e. LTRA, LAMA)
  1. Ability to take oral medication and be willing to adhere to the regimen

  2. Ability to speak and read English

  3. If female and sexually active, should use effective forms of birth control

Exclusion Criteria:
  1. Current use of turmeric (curcumin) or use within the last 7 days

  2. Current use of biologic therapy/ immunotherapy/ or bronchothermoplasty

  3. Pregnancy or lactation

  4. Known allergic reactions to components of turmeric (curcumin)

  5. Current use of anticoagulants, and history of coagulopathy or liver disease

  6. INR greater than 2.0, PTT greater than 45.0 seconds

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Loma Linda University

Investigators

  • Principal Investigator: Laren Tan, MD, Loma Linda University Health

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Loma Linda University
ClinicalTrials.gov Identifier:
NCT04353310
Other Study ID Numbers:
  • 5190424
  • 145101
First Posted:
Apr 20, 2020
Last Update Posted:
Nov 17, 2021
Last Verified:
Nov 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
Yes
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Loma Linda University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 17, 2021