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Randomized, controlled study comparing two mouthwashes with regard to taste assessment and reduction of oral mucosa in oncological patients " - Octenidol® vs. Glandomed®

Randomized, controlled study comparing two mouthwashes with regard to taste assessment and reduction of oral mucosa in oncological patients " - Octenidol® vs. Glandomed® - mucoglan

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00011318
Enrollment
110
Registered
2016-11-17
Start date
2008-10-01
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

mucositis K12.3

Interventions

Group 1: Patients with oncological primary disease and stem cell transplantation Mouthwash solution with Glandomed(Chlorhexidine digluconate) according to individual maintenance plan (5 x mouthwash) f

Sponsors

Fa. Schülke GmbH
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: • Participants> 18 years • Signed declaration of consent to participate or Written declaration of consent by the supervisor • German speaking • oncological patients (KMT autologous or allogeneic)

Exclusion criteria

Exclusion criteria: • Mental disorders • Existing mucositis before radiation therapy / chemotherapy • Current therapy with chemotherapy or irradiation • Incompatibility with CHX or octenidine • Temperatures> 38 degrees Celsius before irradiation / chemotherapy • Dental defect or loose teeth • Infection of the upper respiratory tract

Design outcomes

Primary

MeasureTime frame
State of mucositis by standardc scores.OMAS-Skala (Oral mucositis assessment scoale) and WHO-Skala zur Mucositis)The parameters are measured at three times in day 0, day 3, day 5 and day 14 in the morning)

Secondary

MeasureTime frame
Pain (visuel analogue scale), difficulties in swallowing, temperature, microbiological tests of saliva (bacterial material)The parameters are measured at three times, in day 0, day 3 day 5 and day 14 in the morning)

Countries

Germany

Contacts

Public ContactThomas Neubert

Universitätsklinikum Giessen und Marburg GmbH

neubertt@med.uni-marburg.de064215863285

Outcome results

None listed

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