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Effect of pippermint on nausea in pediatrics with leukemia undergoing chemotherapy

Phase 3
Recruiting
Conditions
ausea, vomiting and Anorexia.
Nausea and vomiting
Registration Number
IRCT20171203037733N4
Lead Sponsor
Arak University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
68
Inclusion Criteria

Written conset to participate in the study
Definitive diagnosis of myeloid leukemia and acute lymphocytic (ALL and AML) by a pediatric hematologist and oncologist (other than None M3ALL )
Receiving chemotherapy courses
History of receiving at least one course of chemotherapy
Experience of nausea following previous chemotherapy sessions
No concomitant radiotherapy with chemotherapy
Age 3 to 18 years

Exclusion Criteria

Using medications or other treatments to reduce nausea other than the usual prescribed anti-nausea and vomiting medications (especially herbal remedies)
Nausea and vomiting resistant to treatment
Unwillingness to participating in the study
sensitivity to mint
other nausea problems such as hypertention , liver failure , kidney and digestive problems

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
ausea. Timepoint: Before, immediately, 24 hours, 48 hours after chemotherapy. Method of measurement: VAS questionnaire and measurement table and Face scale.;Vomiting. Timepoint: Before, immediately, 24 hours, 48 hours after chemotherapy. Method of measurement: VAS questionnaire and measurement table and Face scale.;Anorexia. Timepoint: Before, immediately, 24 hours, 48 hours after chemotherapy. Method of measurement: VAS questionnaire and measurement table and Face scale.
Secondary Outcome Measures
NameTimeMethod
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