Skip to content

Effect of aloe vera on chemotherapy induced stomatitis

The effect of Aloe vera mouthwashe on the intensity of stomatitis and related pain in all patients with leukemia and lymphoma who receiving chemotherapy refferd to hospitals affiliated to Shiraz University of Medical Science.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014092819318N1
Enrollment
64
Registered
2014-11-02
Start date
2014-08-23
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: AML. Condition 2: ALL. Acute Myeloblastic Leukaemia Acute Lymphoblastic Leukaemia

Interventions

Intervention 1: interventional group: prescription of aloe vera mouthwashe. for 2 weeks and 3 time daily, using 5 cc of aloevera mouthwashe each time. Intervention 2: patient will used commonly prescr
Treatment - Drugs
interventional group: prescription of aloe vera mouthwashe. for 2 weeks and 3 time daily, using 5 cc of aloevera mouthwashe each time.
patient will used commonly prescribed mouthwashes in hemathology and oncology departments for 2 weeks and 3 times/ day 5 cc each times.

Sponsors

Shiraz University of Medical Science and Health Services
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Main inclusion criteria: Willingness to participate in the study; Minimum age of 18 years; New diagnosed cancer with AML and ALL; Absence of underlying disease; No addiction to cigar,tobacco; The lack of context sensitivity on aloe vera. Main exclusion criteria: food allergy to the substances during the study; A ciritical condition during the study that causes patients exclusion.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Intensity of stomatitis. Timepoint: 5 visit in 2 weeks, in 1th, 3th,5th,7th,14th days. Method of measurement: stomatitis scale provided by WHO.;Stomatitis related pain. Timepoint: 2 weeks, 5 visit in 1th,3th,5th,7th,14th days. Method of measurement: VAS.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMA Parisa Mansoori

School of Nursing-Midwifery Fatemem

mansoorip@sums,ac,ir+98 71 3647 4254

Outcome results

None listed

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