G25.3
Conditions
Interventions
Group 1: Patients (all age groups) with chronic singultus (> 3 months) who have been or will be admitted to the Centre for Chronic Singultus at the University Hospital of Heidelberg will be included i
Sponsors
Klinik für Anästhesiologie, Universitätsklinikum Heidelberg
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients with chronic singultus who are able to give consent and are affiliated with the Centre for Chronic Singultus at Heidelberg University Hospital, all age groups. This includes both patients presenting for the first time and patients presenting to the centre again.
Exclusion criteria
Exclusion criteria: Refusal to participate in the study by the patient or, in the case of minors, also by the parents, lack of consent, insufficient understanding of the German language by the patient or, in the case of minors, by the parents.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| This is a registry study. A primary endpoint has not been defined. However, in a first step, a statistically descriptive evaluation of the patients connected to the Centre for Chronic Singultus will be carried out in the sense of a real-world data analysis. | — |
Secondary
| Measure | Time frame |
|---|---|
| This is a registry study. A secondary endpoint has not been defined. However, in a second step, a longituginal observation of patients with chronic singultus is to be made possible. | — |
Countries
Germany
Contacts
Public ContactMarco Zugaj
Klinik für Anästhesiologie, Universitätsklinikum Heidelberg
Outcome results
None listed