This clinical trial focused on children aged 4 to 15 years with migraines who were referred to the pediatric neurology clinic at Besat Hospital in Hamadan, Iran, during 2019 - 2020. The study included those eligible for migraine prophylaxis.
Initially, a constipation diagnosis questionnaire based on the Rome IV diagnostic criteria was completed for the patients, and 32 patients with concurrent functional constipation were enrolled in the study. These children were then randomly divided into intervention and control groups.
The intervention group, consisting of 16 patients, received treatment for functional constipation in addition to propranolol (manufactured by Razak Company) at a dosage of 1 mg/kg, with a maximum daily dose of 80 mg. The control group, also comprising 16 patients, was treated solely with propranolol (manufactured by Razak Company).
The functional constipation treatment included dietary changes and the administration of Pidrolax powder without electrolytes (produced by Sepidaj Company) at a dosage of 0.7 g/kg twice daily, with the maximum dosage ranging from 13.8 to 40 g/day. For children with rectal impaction, a 5 mg Bisacodyl suppository was used daily for 3 - 5 days. Throughout the study, patients were not permitted to use any additional treatments for constipation.
The diagnosis of rectal impaction was determined through abdominal examination, digital rectal examination, and, when necessary, plain abdominal radiography. A successful response to constipation treatment was defined as achieving 1 to 3 painless bowel movements per week in the last month of treatment and a reduction in the frequency of fecal incontinence to fewer than 2 episodes per month.
Before initiating treatment, a questionnaire was completed to gather patient information and details about headache characteristics, such as the frequency of headaches in the past month and the duration of headache attacks. At the end of the first month, the questionnaire on headache characteristics was revisited, along with an additional questionnaire to evaluate the response to constipation treatment. Additionally, a 5-point Likert scale checklist was used to assess parental satisfaction with the treatment. The inclusion criteria for the study were as follows: (1) Age between 4 to 15 years; (2) diagnosis of migraine headache by a pediatric neurologist based on the ICHD III β criteria; (3) diagnosis of functional constipation by a pediatric gastroenterologist according to the Rome IV criteria; (4) eligibility for migraine prophylaxis with propranolol, indicated by frequent headaches occurring more than once a week or more than 4 times a month, unsatisfactory response to symptomatic treatments, or presence of debilitating headaches leading to school absenteeism, dysfunction at home, or disruption of the child's social activities.
The exclusion criteria were: (1) The presence of contraindications to receiving propranolol, such as a history of asthma, liver disease, diabetes mellitus, bradycardia, heart block, or severe blood pressure drop; (2) lack of satisfaction or cooperation in participating in the study.
In this study, the chi-square test (or Fisher's exact test) was utilized to compare qualitative variables, while the Mann-Whitney test was applied to compare quantitative variables. Data analysis was conducted using SPSS statistical software version 20, with a significance level set at less than 0.05. The Ethics Committee of Hamadan University of Medical Sciences approved this study, assigning the ethics code from the Deputy of Research and Technology, IR.UMSHA.REC.1398.951, and the IRCT number IRCT20120215009014N361.
Prior to commencing the study, written informed consent was obtained from all participants or their parents.