Comparison of ginger and nystatin mouthwashes on denture stomatitis

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2014011616246N1

Enrollment

Registered

2015-01-17

Start date

2014-09-23

Completion date

Unknown

Last updated

2018-02-22

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

Conditions

denture stomatitis. Candidal stomatitis Oral thrush

Interventions

Intervention 1: Intervention group: the members of this group (15 people) will be presented ginger mouthwash, produced by Rozhin Company (Tabriz, Iran). Each person must use mouth washes 4 times daily

Treatment - Drugs

Intervention group: the members of this group (15 people) will be presented ginger mouthwash, produced by Rozhin Company (Tabriz, Iran). Each person must use mouth washes 4 times daily, each time 20 d

Control group: the members of this group (15 people) will be presented nystatin mouthwash, produced by Jabir Ibn Hayyan pharmaceutical Company (Tehran, Iran). Each person must use mouth washes 4 times

Eligibility

Sex/Gender

All

Age

30 Years to 100 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1 . Erythematose denture stomatitis patients. 2 . Willingness to participate in the study. 3 . Masticatory muscle health.(on The clinical examination of the masticatory muscles , tenderness and trismus Should not be seen). 4 . The ability to use mouthwash. 5 . Mental health. 6 . Denture fit(no signs of loose discoloration ) Exclusion criteria : 1 . A history of using antifungal drugs, antibiotics, and corticosteroid within the previous month. 2 . Allergy to ginger and nystatin mouthwashes. 3 . Alzheimer’s disease. 4 . Unwillingness to participate in the study. 5 . People with neuromuscular diseases who have no ability to oral hygiene. 6 . people with pinpoint and granular denture stomatitis 7 .People who are not qualified to give personal satisfaction (Such as children and people with mental disabilities).

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
The length of erythem. Timepoint: On days: 0 ,5 ,10 ,15 ,20 of study. Method of measurement: Digital dial caliper, in hundredths of a millimeter.	—

Secondary

Measure	Time frame
The width of erythem. Timepoint: On days: 0 ,5 ,15 ,20 of study. Method of measurement: Digital dial caliper, in hundredths of a millimeter.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Hosein Eslami

Tabriz Dental College

eslamih@tbzmed.ac.ir; aylinpakroo@yahoo.com; pakroo.solmaz@gmail.com+98 41 3335 5965

Outcome results

None listed

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