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Ciprofloxacin in Drug-resistant Epilepsy (CIDRE)

M

Mazandaran University of Medical Sciences

Status

Completed

Conditions

Epilepsy Intractable

Treatments

Drug: Ciprofloxacin Oral Product

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

This study aims to investigate the effect of a short-term prescription of ciprofloxacin on intestinal microbial pattern and seizure frequency of patients with drug-resistant epilepsy.

Enrollment

23 patients

Sex

All

Ages

16 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Drug-resistant epilepsy with frequency of at least 2 seizure/Week
  • Acceptance of patients or his/her guardian (Signing informed consent)

Exclusion criteria

  • Hypersensitivity to ciprofloxacin or other fluoroquinolones
  • History of tendon, renal, hepatic or cerebrovascular disease, organ transplantation or myasthenia gravis
  • Usage of medications with interaction to ciprofloxacin
  • No reliable contraception
  • Pregnancy or breastfeeding
  • Being under treatment with corticosteroid
  • Usage of antibiotics in recent 2 months or need to use it during the study
  • Patients who are candidate for epilepsy surgery or other nonmedical treatments
  • Change in anti-seizure medications (ASMs) during recent month
  • Patients who will need changes in ASMs dose during study

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

23 participants in 1 patient group

Ciprofloxacin
Other group
Treatment:
Drug: Ciprofloxacin Oral Product

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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