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Topical Capsaicin for Cyclical Vomiting

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Henry Ford Health

Status and phase

Completed
Phase 2

Conditions

Cyclical Vomiting

Treatments

Drug: Placebos
Drug: Capsaicin 0.1% Cream

Study type

Interventional

Funder types

Other

Identifiers

NCT03223350
10658 (Registry Identifier)

Details and patient eligibility

About

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

Enrollment

30 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

30 participants in 2 patient groups, including a placebo group

Capsaicin
Experimental group
Description:
0.1% capsaicin cream, one application
Treatment:
Drug: Capsaicin 0.1% Cream
Placebo
Placebo Comparator group
Description:
Topical cream with no active drug
Treatment:
Drug: Placebos

Trial documents
2

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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