dyspepsia. Somatoform autonomic dysfunction
Conditions
Interventions
Intervention 1: Cases is prescribed standardized ginger and quince capsules three times a day, within 15 minutes of each meal, starting from 3 days before chemotherapy until completion of radiotherapy
Treatment - Drugs
Placebo
Cases is prescribed standardized ginger and quince capsules three times a day, within 15 minutes of each meal, starting from 3 days before chemotherapy until completion of radiotherapy period ( six we
Control group is prescribed placebo (lactose- bran compound) three times a day, within 15 minutes of each meal, starting from 3 days before chemotherapy until completion of radiotherapy period ( six w
Sponsors
Simorgh-e-Hekmat knowledge-base institute
Research vice-chancellor, Tehran university of medical sciences and health services
Eligibility
Sex/Gender
All
Age
18 Years to 139 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: suffering from cancer; definitely diagnosed by a pathologist; 18?? year-old or more; under chemotherapy treatments; simultaneous radiotherapy treatments inducing ?nausea and vomiting such as whole body or upper abdomen. Exclusion criteria: Warfarin and Heparin ?treatment; ASA consuming more than 80 mg; history of? blood disorders; history of severe thrombocytopenia; allergy to ginger or consuming it during the ?past week; gastro-intestinal cancers; having nausea and vomiting induced by factors except ?chemotherapy or radiotherapy such as CNS tumors, HTN, renal failure or hepatic disorders; gastrointestinal ?problems like gastric or peptic ulcers; forgetting the use of capsules three consecutive times or more.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Nausa. Timepoint: During the intervention, weekly. Method of measurement: Data registration form.;Vomiting. Timepoint: During the intervention, weekly. Method of measurement: Data registration form.;Bloating. Timepoint: During the intervention, weekly. Method of measurement: Data registration form.;Anorexia. Timepoint: During the intervention, weekly. Method of measurement: Data registration form.;Poor appetite. Timepoint: During the intervention, weekly. Method of measurement: Data registration form.;Postprandial fullness. Timepoint: During the intervention, weekly. Method of measurement: Data registration form. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMahdiyeh Falamarzi
Medicin college, Tehran university of medical sciences and health services
Outcome results
None listed