Author/Authors :
Kamalinejad Mohammad نويسنده , Abrishamkar Mahboobeh نويسنده Urology Division, Brain and Spinal Injury Research Center (BASIR), Tehran University of Medical Sciences, Tehran, Iran , Chaibakhsh Samira نويسنده Biostatistics and Epidemiology Division, Brain and Spinal Injury Research Center (BASIR), Tehran University of Medical Sciences, Tehran, Iran , Jafari Rozita نويسنده Imam Reza Teaching Hospital, Tabriz University of Medical Sciences, Tabriz , Karimi Mehrdad نويسنده Traditional Medicine Departments, Faculty of Tradition Medicine , Ghorbani Jahangir نويسنده Dept. of Otolaryngology, Head and Neck Surgery, Tracheal Research Center, Masih Daneshvari Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran , Emtiazy Majid نويسنده Faculty of Iranian Traditional Medicine, Traditional Medicine Faculty, Shahid Sadoughi university of medical Sciences, Ardakan, Yazd, Iran , Jafari Zahra نويسنده Cognitive Neuroscientist, Ph.D. Rehabilitation Research Center (RRC), Department of Basic Sciences in Rehabilitation, School of Rehabilitation Sciences, Iran University of Medical Sciences
Abstract :
Background According to the Iranian Traditional Medicine (ITM)
resources, myrtle (Myrtus communis L.) resolves
swelling, wounds and injuries; its wound exsiccation capability and
tissue enforcement properties may be helpful in the treatment of the
rhinosinusitis. Objectives The objective of the current trial was to
assess the effects of Myrtus communis aqueous extract
in the treatment of chronic rhinosinusitis. Methods A total of 38
patients referring to the Masih Daneshvari Hospital (Tehran, Iran) for
the treatment of chronic rhinosinusitis during the year 2016 were
recruited for a double-blinded randomized placebo-controlled trial. They
were randomly allocated in 2 groups: 22 patients were in the treatment
group and 16 patients in the placebo group. Recruitment was based on the
European position paper on rhinosinusitis (EPOS). Patients’ data,
including demographic information, SNOT22 questionnaire scores, and
visual analog scale (VAS), were gathered and recorded by an
otolaryngologist. Patients were investigated with a CT scan of the
paranasal sinuses at the beginning of the study. Results A total of 13
patients (59.1%) in the treatment group were female and 7 in the placebo
group (43.7%). The median age of patients in the treatment group was
38.86 (18 - 68) and in the placebo group 39.93 (22 - 75) years. Data
analysis revealed that symptoms improved in the treatment group after
treatment in most parameters, according to the SNOT- 22 parameters.
However, most of these improvements, such as reduced concentration (1.81
± 2.01 vs. 0.73 ± 1.32 in control vs. treatment group, respectively; P =
0.055), frustrated/restless/irritable (1.56 ± 1.97 vs. 0.55 ± 1.1 in
control and treatment groups, respectively; P = 0.113), as well as ear
pain (P = 0.121), did not demonstrate a statistical significance. There
was a significant improvement in symptom number 18 (reduced
productivity) in the SNOT- 22 questionnaire (1.69 ± 1.92 vs. 0.77 ± 1.23
in control vs. treatment group, respectively; P = 0.041). Conclusions
According to the present study findings, Myrtus
communis L. syrup can be safely administered in patients with
chronic rhinosinusitis and is effective in improving the outcomes of the
disease.