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HiccupNCT05313685

Educational Materials for Hiccups

An observational study of Hiccup, run by Mayo Clinic at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This is a research study about hiccup educational materials. The purpose of this study is to learn whether this type of research can be done. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Hiccup
How many people
50 participants
Where
1 siteUnited States
Study dates
6 Dec 2021to 25 Mar 2022
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Patients who have had hiccups in the preceding four weeks or patients who might be at risk for hiccups based on drug exposure (for example, recent dexamethasone exposure).

Who may be able to join

  • Age ≥ 18 years of age.
  • Hiccups in the 4 weeks prior to phone contact (patient must confirm).
  • Able to speak and read English.
  • Has an e-mail address.

Who cannot join

  • Individuals < 18 years of age.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Mayo Clinic Rochester

    Rochester, Minnesota, 55905

Other trials in United States

About this study

Official title: A Feasibility Double-Blinded, Randomized Study of Educational Materials for Hiccups

This is a research study about hiccup educational materials. The purpose of this study is to learn whether this type of research can be done.

Conditions
Hiccup
Medical subject headings
Hiccup

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT05313685
Study groupRoleWhat they receive
Mayo Clinic hiccup educational materialsNot described
Mayo Clinic hiccup educational materials + updated supplementary contentNot described

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Feasibility of enrollment

    This is a feasibility study that seeks to enroll 20 patients with hiccups in 5 months from the start of trial recruitment.

    Measured: 5 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Apr 2022
  2. Study start6 Dec 2021
  3. Primary completion23 Feb 2022
  4. Study completion25 Mar 2022

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
50 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05313685
Sponsor's protocol ID
21-012057
Status last verified
Jun 2022
First submitted
28 Mar 2022
Last updated
22 Jun 2022
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Hiccup, run by Mayo Clinic at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 22 Jun 2022. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Feasibility of enrollment (time frame: 5 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Jun 2022.

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