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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03223350
Other study ID # 10658
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date December 20, 2017
Est. completion date August 5, 2019

Study information

Verified date December 2021
Source Henry Ford Health System
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a phase 2 randomized controlled trial testing the effect of topical capsaicin for the relieve of nausea and vomiting.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date August 5, 2019
Est. primary completion date August 5, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - suspected cyclical vomiting syndrome / cannabinoid hyperemesis - active severe nausea or vomiting in the emergency department Exclusion Criteria: - pregnant women, children < 18 years, no prior history of similar symptoms, suspected surgical or infectious cause of symptoms, suspected hepatitis or pancreatitis, allergy to capsaicin or hot peppers, chronic use of prescription antiemetic in prior 24 hours, abdominal pain alone (without nausea or vomiting)

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Capsaicin 0.1% Cream
Topical application
Placebos
placebo cream

Locations

Country Name City State
United States Henry Ford Hospital Detroit Michigan

Sponsors (1)

Lead Sponsor Collaborator
Henry Ford Health System

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Nausea Visual Analog Scale Nausea visual analog scale, ranging from 0-100 mm, high measurement indicates worse nausea 30 minutes
See also
  Status Clinical Trial Phase
Enrolling by invitation NCT05812339 - Body Surface Gastric Mapping to Evaluate Patients With Upper Gastrointestinal Symptoms and Controls