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Examination of postoperative dysosmia and dysgeusia after nasal intubation of patients in the maxillofacial surgery

Examination of postoperative dysosmia and dysgeusia after nasal intubation of patients in the maxillofacial surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00022265
Enrollment
54
Registered
2020-10-20
Start date
2020-06-29
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

R43.8

Interventions

Group 1: Patients with postoperative dysosmia and dysgeusia after nasal intubation. Group 2: Patients with similar operating conditions but with oral intubation. We do not give these patients any smel

Sponsors

Universitätsklinikum Düsseldorf
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: All patients who experience dysosmia and dysgeusia postoperatively.

Exclusion criteria

Exclusion criteria: Alcohol and substance abuse Nasal infection or deformation Congenital, neurological, endocrinological and mental illnesses Traumas of the midface or cranium in the past 6 months

Design outcomes

Primary

MeasureTime frame
The goal is to prove the causality between nasal intubation and loss of smell / taste. For this, all parameters under which the operation was carried out are compared. Afterwards, post-operative tests are carried out with so-called “sniffing sticks” to make the results comparable.

Secondary

MeasureTime frame
Another goal is to find out whether smell training can improve or remedy dysosmia. For this, the patients receive a "fragrance quartet" with which they train their sense of smell every day. After six months, another test is carried out with the “sniffing sticks” to observe the development.

Countries

Germany

Contacts

Public ContactKlara Lempert

Universitätsklinikum Düsseldorf

Kllem100@hhu.de02118118189

Outcome results

None listed

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