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NCT Number: NCT01125241

A Study to Evaluate the Efficacy and Safety of Add-on Therapy of Wuling Capsule in Epilepsy Patients With Depression

The main purpose of this study is to determine the effects of add-on therapy of wuling capsule on depressive symptoms in patients with comorbidity of epilepsy and depression, to evaluate its influences on the frequency and severity of seizures, and to observe its effects on patients' sleeping condition, quality of life.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Peking Union Medical College Hospital, Beijing, China, Beijing, Beijing Municipality, China

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About this study

The phenomenon of epileptic patients who have psychiatric disorders is very common, of which the prevalence of depression is the highest and depression is also an independent risk factor affecting epileptic patients' quality of life. Due to some social factors, non-typical clinical symptoms and limited therapeutic methods(tricyclic antidepressants, lithium chloride and 5-serotonin uptake inhibitors may all have risks of lowing threshold of seizures), epileptic patients with depression are usually not be recognized and treated properly. Wuling capsule has been used in therapy of insomnia, nervous breakdowns and a previous small sample clinical trial revealed that it could improve mood disorders of epileptic patients and hadn't affected severity of seizures (not published). Therefore a multi-center, randomized, double-blinded and placebo-controlled superiority clinical trial will be carried out to determine the effects of add-on therapy of wuling capsule on depressive symptoms in patients with epilepsy, to evaluate its influences on the frequency and severity of seizures, and to observe its effects on patients' sleeping condition, quality of life.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Subjects for this study will meet the following criteria:

  • Age greater than or equal to 18 years.
  • Must be in accordance with the diagnostic criteria of epilepsy and have taken antiepileptic drugs regularly at least for 6 months, which will not be changed recently. The duration to the latest seizure must be longer than 24 hours.
  • Score of a 17 item Hamilton Depression is greater than or equal to 17 and depressive symptoms have lasted for at least 2 weeks.
  • Haven't taken any anti-anxiety, anti-depressant and anti-psychotic drugs in recent 2 weeks.
  • Must sign the informed consent form.

Exclusion criteria

  • Now accepting or have accepted other drugs clinical trial in the last month.
  • History of serious psychiatric illness other than depression.
  • Having suicide ideas or suicide behaviors.
  • Progressive illness of central nervous system, such as degenerative disease or tumor.
  • History of serious cardiac or pulmonary disease, hepatic and renal dysfunction, and malignant tumors.
  • The value of ALT or AST is higher than 1.5 times normal range, or the number of white blood cells is less than 2500/ul, or the number of neutrophil granulocyte is less than 1000/ul.
  • During pregnant or lactation period.
  • The person who is disabled or mentally disabled.

Treatment and study plan

Wuling Capsule

Drug

orally, three tablets each time,three times a day

placebo of wuling capsule

Drug

orally, three tablets each time and three times a day

Primary outcomes

  1. symptoms of depression using the 17-item Hamilton Depression Rating Scale (HDRS)

    Time frame: 3 months

Secondary outcomes

  1. the frequency of seizures using diary

    Time frame: 3 months

  2. the severity of seizures using the National Hospital Seizure Severity Scale(NHS3)

    Time frame: 3 months

  3. the sleeping condition using Pittsburgh Sleep Quality Index (PSQI)

    Time frame: 3 months

  4. the quality of life using Quality of Life in Epilepsy (QOLIE-31)

    Time frame: 3 months

Sponsors and collaborators

Lead sponsor

Shanghai Zhongshan Hospital

Other

Collaborators

  • Shanghai Ankang Pharmaceutical Co.,LTD
  • Shanghai Wu Mengchao Medical Foundation

Registry information

Official study title

A Study to Evaluate the Efficacy and Safety of Add-on Therapy of Wuling Capsule in Epilepsy Patients With Depression: a Muli-center, Randomized, Double-blinded, Placebo-controlled Superiority Clinical Trial

Important dates

Study start
2010
Primary completion
2013
Study completion
2013
First posted
May 18, 2010
Registry last updated
Sep 17, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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