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Hypogeusia In Vim/DRT-DBS

Hypogeusia In Vim/DRT-DBS - HIDDen

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00012931
Enrollment
30
Registered
2017-09-08
Start date
2017-10-18
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

G25.0 R43.8

Interventions

Group 1: Pre-operative gustometry, olfactometry and rhinomanometry prior to implantation of DBS (Deep Brain Stimulation) system. Post-operative gustometry, olfactometry and rhinomanometry 6-12 months

Sponsors

Universitätsklinikum FreiburgKlinik für NeurochirurgieAbteilung für Stereotaktische und Funktionelle Neurochirurgie
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Adult tremor patients who are being treated with DBS and where DTI imaging data is available. Decision for DBS therapy is made according to standard guidelines outside this study. 2. Written informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients suffering from multiple sclerosis. 2- Patients with allergies on citric acid or chinine.

Design outcomes

Primary

MeasureTime frame
To compare gustatory and olfactory function by means of olfactometry and gustometry preoperatively as well as 6-12 months after Implantation of DBS (Deep Brain Stimulation)

Secondary

MeasureTime frame
Identification of risk factors for stimulation-induced hypogeusia (age, sex, pre-existing disturbance of olfaction or gustation).

Countries

Germany

Contacts

Public ContactBastian Sajonz

Universitätsklinikum FreibugKlinik für NeurochirurgieAbteilung für Funktionelle und Stereotaktische Neurochirurgie

bastian.sajonz@uniklinik-freiburg.de+49 761 270 50010

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026