The effect of combined mouthwash on chemotherapy-induced ulcer

Study of the effect of the combined mouthwash (dalen) on treatment of stomatitis in patient undergoing chemotherapy

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20171203037737N2

Enrollment

Registered

2018-07-06

Start date

2018-07-23

Completion date

Unknown

Last updated

2018-09-11

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

Conditions

Palliative care. Encounter for palliative care

Interventions

Intervention 1: Intervention group: Intervention group: Using a combination of mouthwash (Dilute Nitatin 12 ml / Diphenhydramine 100 ml Syrup / Aloe Minim MJ 240 ml). Intervention 2: Control group: (A

Eligibility

Sex/Gender

All

Age

18 Years to 68 Years

Inclusion criteria

Inclusion criteria: Have acute leukemia and lymphoma cancers and are undergoing periodic chemotherapy. When entering the study, there is no have stomatitis.

Exclusion criteria

Exclusion criteria: Having asthma and other allergic diseases Radiation therapy is also associated with chemotherapy. During the study, they develop a systemic infection.

Design outcomes

Primary

Measure	Time frame
Occurrence of osteomathitis in patients undergoing chemotherapy. Timepoint: On day one, seventh and fourth sessions in two groups after intervention. Method of measurement: Nominal(was observedwas not observed).;Severity of osteomathia in patients undergoing chemotherapy. Timepoint: On day one, seventh and fourth sessions in two groups after intervention. Method of measurement: There is no wound in the first degree. The second grade involves wound healing, but the person has the ability to eat.Grade 3 is large (more than 25% of the mouth level), and the individual has only the ability to eat the Maya.. In grade 4, hemorrhagic fever is bleeding and the patient is unable to receive the substance.;Treatment time of osteomyte in patients undergoing chemotherapy. Timepoint: On day one, seventh and fourth sessions in two groups after intervention. Method of measurement: ased on the time of recovery symptoms of time-to-day.	—

Measure

Time frame

Occurrence of osteomathitis in patients undergoing chemotherapy. Timepoint: On day one, seventh and fourth sessions in two groups after intervention. Method of measurement: Nominal(was observedwas not observed).;Severity of osteomathia in patients undergoing chemotherapy. Timepoint: On day one, seventh and fourth sessions in two groups after intervention. Method of measurement: There is no wound in the first degree. The second grade involves wound healing, but the person has the ability to eat.Grade 3 is large (more than 25% of the mouth level), and the individual has only the ability to eat the Maya.. In grade 4, hemorrhagic fever is bleeding and the patient is unable to receive the substance.;Treatment time of osteomyte in patients undergoing chemotherapy. Timepoint: On day one, seventh and fourth sessions in two groups after intervention. Method of measurement: ased on the time of recovery symptoms of time-to-day.

—

Secondary

Measure	Time frame
Gum wound healing. Timepoint: On day one, seventh and fourth sessions in two groups after intervention. Method of measurement: prpportional.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNasrin Elahi

Ahvaz University of Medical Sciences

Elahi-n@ajums.ac.ir+98 61 3373 8621

Outcome results

None listed

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