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Laser effect in preventing the incidence of chemotherapy-induced oral ulcers in patients with acute leukemia

Low level laser effect in preventing the incidence of chemotherapy-induced oral mucositis in patients with acute leukemia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201110157801N1
Enrollment
40
Registered
2011-10-23
Start date
2011-10-23
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

Condition 1: acute lymphoblastic leukemia. Condition 2: acute myeloid leukemia. Acute lymphoblastic leukaemia Acute myelblastic leukaemia

Interventions

Intervention 1: For all participants in both groups, a prophylactic phase will be started from the first day of chemotherapy. In this phase standard oral hygiene will be recommended, furthermore chlor
Prevention
For all participants in both groups, a prophylactic phase will be started from the first day of chemotherapy. In this phase standard oral hygiene will be recommended, furthermore chlorhexidine 0.12%,
In intervation group, low level laser (660nm, 25 mw and 1.5 J/cm2) will be applied on 18 different points in the mouth, 2 times a week during chemotherapy.

Sponsors

Dental faculty, Shiraz university of medical sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 12-70 y/o; both genders; suffering acute myeloid/lymphoblastic leukemia; receiving myeloablative chemotherapy regimen; healthy oral mucosa at before starting chemotherapy; able to cooperation; filling the informed consent form. Exclusion criteria: unhealthy oral mucosa (erythema, ulcer, soreness) before starting chemotherapy; non ablative chemotherapy regimen; inability or unwillingness for being involved.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Reducing the incidence of ulcer and erythema. Timepoint: 1 week, 2 weeks, 3 weeks, 4 weeks. Method of measurement: observation of the erythema and ulcer accordig to WHO & NCI scale.

Secondary

MeasureTime frame
Reducing pain. Timepoint: 1 week, 2 weeks, 3 weeks, 4 weeks. Method of measurement: explaining the amount of pain according to the patients' expression (1-10 numbers).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Mohammad Mehdi Fani

Oral medicine department, Dental faculty

mogharabis@sums.ac.ir+98 71162631934

Outcome results

None listed

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