The effect of Glutamine Oral gel onprevention of chemotherapy-induced mucositis

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT201411153106N19

Enrollment

Registered

2014-12-12

Start date

2014-11-22

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

Oral mucositis. Oral mucositis (ulcerative)

Interventions

Intervention 1: Intervention group: general oral care with glutamine oral gel, from the first day up the end of cycle for 3 cycles. Patients were assessed at baseline and at the end of each cycle usin

Treatment - Drugs

Intervention group: general oral care with glutamine oral gel, from the first day up the end of cycle for 3 cycles. Patients were assessed at baseline and at the end of each cycle using visual examina

Control group: general oral care

Eligibility

Sex/Gender

All

Age

20 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: consciousness; being literate; chemotherapeutic management with drugs which induce mucositis; no stomatitis; no oral disease; no renal & liver disorders; no auto immune disease and diabetes; no fever and neutropenia; no recieved antibiotic & narcotic analgesic Exclusion criterion: sensitivity to glutamine oral gel.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Mucositis. Timepoint: At the end of cycle for 3 cycles. Method of measurement: PROMS and OMAS questionnaires.	—

Countries

Iran (Islamic Republic of)

Outcome results

None listed

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