Clinical Utility and Safety of Human Umbilical Cord Mesenchymal Stem Cell Secretome in Drug Resistant Epilepsy Single Center, Non-randomized, Phase I Clinical Trial

Trial statusNot yet recruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18-60
SponsorBaermed

About this trial

The goal of this clinical trial is to learn if Human Umbilical Cord Mesenchymal Stem Cell (HUCMSC) derived secretome injection is safe and effective in patient with epilepsy. The main questions it ams to answer are:

1. How is the relationship between secretome therapy and the reduction in seizure frequency and duration in patients with drug-resistant epilepsy in the adult age group? 2. How does secretome therapy affect EEG and qEEG results in patients with drug-resistant epilepsy in the adult age group? 3. How is the relationship between secretome therapy and the Mini Mental State Examination (MMSE) score in patients with drug-resistant epilepsy in the adult age group? 4. How does secretome therapy affect stress levels as measured by the Perceived Stress Scale (PSS) in patients with drug-resistant epilepsy in the adult age group? 5. How does secretome therapy affect Gait Deviation Index (GDI) scores in patients with drug-resistant epilepsy in the adult age group? 6. How does secretome therapy affect quality of life as measured by the Quality of Life in Epilepsy Inventory (QOLIE-31) in patients with drug-resistant epilepsy in the adult age group?

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Individuals aged 18 to 60 years.

Individuals with a clinical diagnosis of epilepsy confirmed by a neurologist based on internationally accepted criteria.

Individuals with a seizure frequency of at least 6 times in 12 months.

Individuals who have a history of recurrent seizures that are not controlled with standard antiepileptic treatment of at least 2 types of drugs for at least 12 months.

Disqualifiers

Individuals with a history of stroke or evidence of stroke on medical examination.

Individuals who have undergone surgery for the treatment of epilepsy.

Individuals with a history of allergy or hypersensitivity reactions to the secretome or related components.

Individuals with active or uncontrolled autoimmune disease.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Secretome

    Drug

    3 ml Injection of secretome for 4 times two weeks apart

Treatment groups

54 Participants
are divided into 2 treatment groups
Group A: Secretome InjectionExperimental treatment 1 intervention
Group B: Best Treatment PracticeNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Changes frequency and duration of the seizures in drugs resistant epilepsy after two months secretome injections

Patients achieved a response if there are changes in frequency and duration of the seizures in drugs resistant epilepsy after two months secretome injections.Best outcome when the frequency and duration of the seizures less frequent, worst outcome when the frequency and duration of the seizures get more frequent

Time frame
From enrollment to the end of treatment at 2 months, From enrollment to the end of study at 8 months
2

Changes in EEG and qEEG (Alpha,Beta, Delta, and Theta wave) results of drugs resistant epilepsy after two months secretome injections

Patients achieved a response if there are changes in EEG and qEEG (Alpha,Beta, Delta, and Theta wave) results in drugs resistant epilepsy after two months secretome injections.Best outcome when the EEG and qEEG (Alpha,Beta, Delta, and Theta wave) get a better results, worst outcome when EEG and qEEG (Alpha,Beta, Delta, and Theta wave) get a worse results

Time frame
From enrollment to the end of treatment at 2 months, From enrollment to the end of study at 8 months

Secondary outcomes

1

Changes in Mini Mental State Examination (MMSE) results of drugs resistant epilepsy after two months secretome injections

Patients achieved a response if there are changes in Mini Mental State Examination (MMSE) results in drugs resistant epilepsy after two months secretome injections.Best outcome when the Mini Mental State Examination (MMSE) get a increase results, worst outcome when Mini Mental State Examination (MMSE) get a decrease results

Time frame
From enrollment to the end of treatment at 2 months, From enrollment to the end of study at 8 months
2

Changes in Perceived Stress Scale (PSS) results of drugs resistant epilepsy after two months secretome injections

Patients achieved a response if there are changes in Perceived Stress Scale (PSS) results in drugs resistant epilepsy after two months secretome injections.Best outcome when the Perceived Stress Scale (PSS) get a increase results, worst outcome when Perceived Stress Scale (PSS) get a decrease results

Time frame
From enrollment to the end of treatment at 2 months, From enrollment to the end of study at 8 months
3

Changes in Gait Deviation Index (GDI) results of drugs resistant epilepsy after two months secretome injections

Patients achieved a response if there are changes in Gait Deviation Index (GDI) results in drugs resistant epilepsy after two months secretome injections.Best outcome when the Gait Deviation Index (GDI) get a increase results, worst outcome when Gait Deviation Index (GDI) get a decrease results

Time frame
From enrollment to the end of treatment at 2 months, From enrollment to the end of study at 8 months

Other outcomes

1

Changes in Quality of The Life in Epilepsy Inventory (QOLIE-31) results of drugs resistant epilepsy after two months secretome injections

Patients achieved a response if there are changes in Quality of The Life in Epilepsy Inventory (QOLIE-31) results in drugs resistant epilepsy after two months secretome injections.Best outcome when the Quality of The Life in Epilepsy Inventory (QOLIE-31) get a increase results, worst outcome when Quality of The Life in Epilepsy Inventory (QOLIE-31) get a decrease results

Time frame
From enrollment to the end of treatment at 2 months, From enrollment to the end of study at 8 months

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Baermed

Lead sponsor

Tarumanagara University

Collaborator

This trial is not recruiting at the moment. You can still explore other options: