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Comparison of Propranolol, Flunarizine and Their Combination in Preventing Migraine in Adults in a Tertiary Care Hospital in Bangladesh

17 de junho de 2026 atualizado por: Mohammad Shaifuddin Shourav, Chittagong Medical College

Comparative Efficacy of Propranolol, Flunarizine, and Their Combination in Migraine Prophylaxis: An Open-label Parallel-arm Randomized Controlled Trial

Migraine is a common and disabling neurological condition that affects quality of life, work productivity, and daily functioning. In Bangladesh, migraine is a major health problem, yet access to effective and affordable preventive treatments remains limited. Preventive (prophylactic) treatment is recommended for people who experience frequent migraine attacks in order to reduce the number, severity, and duration of headaches.

Propranolol and flunarizine are two commonly used and relatively inexpensive medications for migraine prevention. Both drugs have been shown to reduce migraine frequency when used alone. However, some patients do not respond adequately to a single medication. Using a combination of drugs that work through different mechanisms may improve treatment effectiveness without significantly increasing side effects. There is limited local evidence comparing propranolol, flunarizine, and their combination in migraine prevention, particularly in the Bangladeshi population.

This study is designed to compare the effectiveness and safety of propranolol alone, flunarizine alone, and a combination of propranolol and flunarizine in preventing episodic migraine in adults. The main hypothesis is that at least one of these treatment strategies, particularly combination therapy, may be more effective than the others in reducing migraine burden.

This is an open-label, parallel-arm, randomized controlled trial conducted at Chittagong Medical College Hospital, Bangladesh. A total of 177 adult patients aged 18 to 55 years who are diagnosed with episodic migraine and experience four or more migraine attacks per month will be enrolled. Participants will be randomly assigned to one of three treatment groups: propranolol, flunarizine, or a combination of both medications. Treatment will be given for 12 weeks, with dose adjustments during the first week and follow-up visits at 6 and 12 weeks.

The primary outcome of the study is the reduction in the number of monthly migraine days. Secondary outcomes include the proportion of patients achieving at least a 50% reduction in migraine days, changes in headache severity and duration, improvement in migraine-related disability (measured by the Migraine Disability Assessment Score), patient-reported treatment satisfaction, and the frequency of side effects.

The results of this study are expected to provide important local evidence to guide clinicians in selecting effective and affordable migraine preventive treatments and to clarify whether combination therapy offers additional benefits over single-drug therapy in routine clinical practice.

Visão geral do estudo

Descrição detalhada

Migraine is a highly prevalent neurological disorder, and in Bangladesh it accounts for approximately 25% of all headache disorders, predominantly affecting individuals aged 15-34 years and imposing a substantial socioeconomic burden through lost work hours and reduced productivity. Propranolol (a non-selective beta-blocker) and flunarizine (a calcium channel blocker) are both established first-line agents for migraine prophylaxis, but head-to-head comparative data in the Bangladeshi population are scarce, and evidence on their combined use remains limited. Prior trials comparing the two agents have produced mixed results, with some favoring flunarizine, others favoring propranolol, and others showing no significant difference. A subset of patients (30-40%) fail to respond adequately to monotherapy, and combination therapy targeting both beta-adrenergic and calcium-channel mechanisms has shown promise in earlier small trials without a clear increase in adverse events.

This study is an open-label, parallel-arm randomized controlled trial conducted in the inpatient and outpatient departments of Neurology and Medicine at Chittagong Medical College Hospital (CMCH), Chattogram, Bangladesh, over a planned duration of 18 months (12-week intervention period per participant, with follow-up at 6 and 12 weeks).

A total of 177 adult patients with episodic migraine (diagnosed per ICHD-3 criteria) will be enrolled using consecutive sampling and randomly allocated via software-generated block randomization (block size of six) with allocation concealment using sealed opaque envelopes, to one of three parallel groups (59 participants per group):

Group 1 (Propranolol): Started at 40 mg daily, increased to 80 mg daily after 7 days.

Group 2 (Flunarizine): Started at 5 mg daily, increased to 10 mg daily after 7 days.

Group 3 (Combination): Propranolol 40 mg plus flunarizine 5 mg daily initially; after 7 days, propranolol maintained at 40 mg while flunarizine is increased to 10 mg daily.

Acute attacks during the study may be managed with naproxen (NSAID) as first-line and zolmitriptan (triptan) if naproxen is ineffective.

At baseline, participants undergo a comprehensive evaluation including demographic data, general and systemic examination, baseline laboratory testing (ECG, RBS, SGPT, SGOT, serum creatinine), migraine history (frequency, duration, severity), MIDAS (Migraine Disability Assessment) score using a Bengali-translated version adopted with author permission, and headache severity (Numeric Rating Scale) and duration. Participants maintain a daily headache diary throughout the study.

Follow-up visits occur at 6 and 12 weeks, during which the headache diary is reviewed, adverse effects are recorded, treatment adherence is assessed by self-report and pill counting [(pills dispensed - pills returned) / pills expected to be taken × 100, with ≥80% considered adherent], MIDAS score is re-assessed at study end, headache severity/duration are reassessed, and Patient Global Evaluation (1-4 Likert scale) is recorded. Vital signs (pulse, blood pressure) and BMI are recorded at each visit. Participants experiencing intolerable adverse effects may be withdrawn and offered alternative treatment.

The primary outcome is the reduction in number of monthly migraine days from baseline to 12 weeks, analyzed using ANCOVA adjusting for baseline values and potential confounders (age, gender, baseline headache frequency), with Bonferroni-corrected pairwise comparisons between the three groups. Secondary analyses include repeated-measures ANOVA for headache severity (NRS), Wilcoxon signed-rank or paired t-tests for MIDAS score change, and Chi-square/Fisher's exact tests for responder rate (≥50% reduction in monthly migraine days at week 12) and adverse effect frequency. Exploratory subgroup analyses by age (<40 vs ≥40 years) and gender will be conducted using ANCOVA or logistic regression as appropriate. Both intention-to-treat and per-protocol analyses will be performed, with missing data handled via ITT principles and multiple imputation if needed. Effect sizes (Cohen's d, partial eta squared) and 95% confidence intervals will be reported for all point estimates. Analyses will be performed using SPSS version 27.0 or later, with statistical significance set at p < 0.05.

Informed consent will be obtained from all participants prior to enrollment. Detailed information about the study's objectives, procedures, potential risks, benefits, and the voluntary nature of participation will be provided in a written format. Participants will be given ample opportunity to ask questions and will be informed that they may withdraw from the study at any time without consequence.

Confidentiality will be maintained at all stages of the study. All participant data will be anonymized using a unique identifier, and personal identifying information will be stored securely. Data will be analyzed and reported in aggregate form to protect participant anonymity. Only authorized personnel will have access to the study data.

A Data Safety and Monitoring Committee (DSMC) will ensure participant safety and the ethical conduct of the trial. The DSMC will periodically review safety data, adverse events, serious adverse events, protocol deviations, dropout patterns, and overall trial progress. If any participant experiences intolerable side effects or other health concerns, appropriate medical intervention will be provided, and the participant will be withdrawn from the study if necessary. Any serious adverse events will be reported to the DSMC and ethics committee in accordance with ethical guidelines.

Finally, the ethical principle of beneficence will be upheld by ensuring that the potential benefits of participation outweigh any risks. The study will aim to improve the management of migraines, leading to better patient outcomes and a more efficient healthcare system, particularly in underserved regions.

Tipo de estudo

Intervencional

Inscrição (Estimado)

177

Estágio

  • Fase 4

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Locais de estudo

      • Chittagong, Bangladesh, 4203
        • Chittagong Medical College
        • Contato:
          • Md. Mahabubul Alam Khandker professor, FCPS (Medicine), MD(Neurology)
          • Número de telefone: +8801711878769
          • E-mail: mahabub1495@gmail.com

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto

Aceita Voluntários Saudáveis

Não

Descrição

Inclusion Criteria:

  1. Participants aged 18 to 55 years.
  2. Diagnosis of episodic migraine, defined according to the International Classification of Headache Disorders, 3rd edition (ICHD-3) criteria.
  3. Participants experiencing 4 or more migraine attacks per month.
  4. Willingness to provide written informed consent to participate in the study.

Exclusion Criteria:

  1. Comorbidities:

    • Presence of other primary headache disorders, chronic migraine, hemiplegic migraine, basilar migraine or any secondary headache disorder.
    • Known serious underlying systemic diseases including Cardiac disease (Heart failure, Heart Block, Arrhythmia), Renal dysfunction, Liver dysfunction, Pulmonary disease (Asthma, COPD), Peripheral vascular disease, Extrapyramidal disease (Parkinson disease, Chorea, Dystonia).
    • Pregnancy or breastfeeding.
    • Psychiatric illness (Depression, Psychosis, Obsessive compulsive disorder).
  2. Medications:

    • Received migraine prophylactic medication within 60 days prior to screening.
    • Use of specific contraindicated medications, including beta-blockers or calcium channel blockers, except as part of the study treatments.
  3. Non-compliance:

    • Inability or unwillingness to comply with study protocols, including maintaining a headache diary or attending follow-up visits.
  4. History of Allergies:

    • Known hypersensitivity to propranolol, flunarizine
  5. Substance Use:

    • Current substance abuse

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Comparador Ativo: Propranolol arm
Participants randomized to this arm will receive propranolol as the sole prophylactic medication for migraine, administered for a total of 12 weeks. Propranolol will be started at 40 mg daily and increased to 80 mg daily after 7 days
Participants randomized to propranolol arm will receive propranolol as the sole prophylactic medication for migraine, administered for a total of 12 weeks. Propranolol will be started at 40 mg daily and increased to 80 mg daily after 7 days
Comparador Ativo: Flunarizine arm
Participants randomized to this arm will receive flunarizine as the sole prophylactic medication for migraine, administered for a total of 12 weeks. Flunarizine will be started at 5 mg daily and increased to 10 mg daily after 7 days
Participants randomized to flunarizine arm will receive flunarizine as the sole prophylactic medication for migraine, administered for a total of 12 weeks. Flunarizine will be started at 5 mg daily and increased to 10 mg daily after 7 days
Comparador Ativo: Combination arm
Participants randomized to this arm will receive a combination of propranolol and flunarizine for migraine prophylaxis, administered for a total of 12 weeks. Treatment will be started at propranolol 40 mg daily plus flunarizine 5 mg daily. After 7 days, the propranolol dose will be maintained at 40 mg daily while the flunarizine dose will be increased to 10 mg daily.
Participants randomized to combination arm will receive a combination of propranolol and flunarizine for migraine prophylaxis, administered for a total of 12 weeks. Treatment will be started at propranolol 40 mg daily plus flunarizine 5 mg daily. After 7 days, the propranolol dose will be maintained at 40 mg daily while the flunarizine dose will be increased to 10 mg daily.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Change in Monthly Migraine Days
Prazo: From baseline to 12 weeks
Monthly Migraine Days refers to the total number of days within a month on which a participant experiences a migraine headache. The change will be measured as the difference between the baseline number of monthly migraine days and the number recorded at the end of the study.
From baseline to 12 weeks

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Responder Rate (≥50% reduction in monthly migraine days)
Prazo: Baseline to 12 weeks
The percentage of patients reporting at least a 50% reduction in their monthly migraine days compared to the baseline. This will be expressed as the percentage of total participants in each treatment arm.
Baseline to 12 weeks
Change in Headache Severity (Numeric Rating Scale)
Prazo: Baseline, Week 6, and Week 12
Intensity of migraine pain rated by participants on a Numeric Rating Scale from 0 (no pain) to 10 (worst pain imaginable), recorded in the headache diary and reviewed at follow-up visits.
Baseline, Week 6, and Week 12
Change in Headache Duration
Prazo: Baseline, Week 6, and Week 12
Length of time (in hours) of each migraine attack, from onset of pain to resolution, as recorded by participants in the headache diary and reviewed at follow-up visits.
Baseline, Week 6, and Week 12
Change in MIDAS (Migraine Disability Assessment) Score
Prazo: Baseline and end of treatment (Week 12)
Score from the Bengali-translated MIDAS questionnaire (adapted from Alam et al., 2018, used with author's permission), measuring migraine-related disability across work/school, household duties, and other daily activities, graded from Grade 1 (minimal disability) to Grade 4 (severe disability).
Baseline and end of treatment (Week 12)
Patient Global Evaluation
Prazo: End of the treatment Week 12
Participant's self-reported overall impression of treatment effectiveness, rated on a 4-point Likert scale (1 = Poor, 2 = Good, 3 = Very good, 4 = Excellent).
End of the treatment Week 12
Frequency of Adverse Effects
Prazo: Throughout the 12-week treatment period (assessed at Week 6 and Week 12)
Number and proportion of participants in each treatment group reporting any adverse effect (harmful or unpleasant effect at therapeutic doses requiring dose reduction or drug withdrawal) during the treatment period, recorded at follow-up visits.
Throughout the 12-week treatment period (assessed at Week 6 and Week 12)

Colaboradores e Investigadores

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Publicações e links úteis

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Publicações Gerais

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Estimado)

1 de julho de 2026

Conclusão Primária (Estimado)

31 de março de 2027

Conclusão do estudo (Estimado)

30 de abril de 2027

Datas de inscrição no estudo

Enviado pela primeira vez

12 de junho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

12 de junho de 2026

Primeira postagem (Real)

18 de junho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

22 de junho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

17 de junho de 2026

Última verificação

1 de junho de 2026

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

produto fabricado e exportado dos EUA

Não

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