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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT03745781
Other study ID # 2018P000294
Secondary ID
Status Terminated
Phase Early Phase 1
First received
Last updated
Start date December 1, 2018
Est. completion date October 7, 2019

Study information

Verified date May 2020
Source Beth Israel Deaconess Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study is evaluating the efficacy of open-label placebo for the treatment of functional dyspepsia.


Recruitment information / eligibility

Status Terminated
Enrollment 21
Est. completion date October 7, 2019
Est. primary completion date October 7, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Functional Dyspepsia

Exclusion Criteria:

-

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Placebos
placebo pills

Locations

Country Name City State
United States Beth Israel Deaconess Medical Center Boston Massachusetts

Sponsors (1)

Lead Sponsor Collaborator
Beth Israel Deaconess Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary dyspepsia severity on a VAS from 0-100 How severe have your dyspepsia symptoms been over the past 7 days (on a VAS from 0-100)? 3 weeks
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