In order to prepare compound drug, in advance, the flowers of A.digitata and M.sylvestris were purchased from an herbal shop in Tehran. They were identified and kept in the herbarium center of school of pharmacy, Tehran University of Medical Sciences with voucher numbers PMP-508 and PMP-509, respectively. Then, both plants were cleaned, powdered, and mixed; then, they were kept in 4 g sachets, containing equal portions. Also, the placebo was prepared from Avicel in form of 4 g sachets, too.
In this triple-blind parallel two-armed randomized clinical trial, 23 patients with H and N cancers, who came for radiotherapy to Imam Hossein hospital oncology clinic, were involved. They recoursed to the clinic from February 2015 to September 2016. The protocol of this investigation was approved by the ethics committee of Shahed University (Code: 41/215586) and registered in the Iranian registry of clinical trials (IRCT2014120520208N1).
Inclusion criteria consisted of age between 17 to 65 years, life expectancy over 1 year, good performance status according to Eastern cooperative oncology group (ECOG) criterion, and a minimum of 4 areas in radiation field. Patients were excluded if they had used alcohol, drugs affecting salivary gland secretions, such as anti-depressants, opioids, anti-hypertensives, anti-histamines, diuretics, mouthwashes, artificial saliva, and cigars, had had the history of chemotherapy and radiotherapy in oropharyngeal region in past 6 months, had had the history of connective tissue diseases, such as Sjogren’s syndrome, Rheumatoid arthritis and Lupus, liver or kidney diseases, major depression, diseases involving salivary glands such as diabetes, diseases causing dehydration, such as chronic diarrhea, immunosuppressive disorders, Myelosuppression, and diseases causing Aphthous ulcers. Patients were excluded too, if they had had mucositis grade 3 or 4, Candidiasis, oral Herpes, failure to treat, need to TPN or hospitalization before getting 50 GY of radiation or did not want to continue the treatment.
Eligible subjects were randomly allocated to 2 groups; those receiving the herbal compound (experimental group) or those receiving placebo (control group) 3 times per day for 7 weeks from beginning of radiotherapy to 2 weeks later.
The herbal compound and the placebo were given to patients by secretary of clinic, and patients, investigators, and statistical analyzer did not know the allocation method during the study until the data analysis.
The protocol of RCT was explained to the patients, and before participating in the study, they studied and signed the written informed consent. Patients were examined at the beginning of the study and followed up each week (2 weeks after completing the radiotherapy). There were both interview and physical examinations of the patients for gathering the required data during their visits. In the first visit, all protocols of the study and prescription of each medication were explained to the patients who met the inclusion criteria. The efficacy of treatment on mouth pain score (MPS) was assessed by using visual analog scale (VAS) and mucositis grade was evaluated by investigator according to WHO scale in every visit. The VAS was scored from 0 to 10, where 0 and 10 denoted the absence of mouth pain and severe mouth pain, respectively.
The collected data compared between 2 groups and more accurate analysis was done, using mixed statistical model with STATA software and the mean MPS; the mucositis of patients of 2 groups were compared in every week. In this integrated analysis, drug effect, time effect and time-drug interaction were surveyed and anywhere the interaction was significant, drug effect in any time, and vice versa, time effect in experimental and control group were analyzed. The p-Value under 0.05 was considered significant.