Hormone Profiles in Adults With Newly Diagnosed Epilepsy
Information source: Chinese University of Hong Kong
Information obtained from ClinicalTrials.gov on November 03, 2008 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Epilepsy
Intervention: Sodium valproate (Drug); Lamotrigine (Drug)
Phase: Phase 4
Status: Recruiting
Sponsored by: Chinese University of Hong Kong Official(s) and/or principal investigator(s): Patrick Kwan, FHKAM, Principal Investigator, Affiliation: Chinese University of Hong Kong
Overall contact: Patrick Kwan, FHKAM, Phone: 852-2632-2211, Email: patrickkwan@cuhk.edu.hk
Summary
Both sodium valproate and lamotrigine are currently used in the treatment of newly diagnosed
epilepsy. Although they appear to have similar efficacy, they have different side effects,
which have not been well studied. This study aims to compare one particular aspect of their
possible side effects, namely whether they affect certain hormonal functions.
Clinical Details
Official title: Hormone Profiles in Adults Treated With Valproate vs. Lamotrigine Monotherapy for Newly Diagnosed Epilepsy: A Prospective Randomised Study
Study design: Treatment, Randomized, Open Label, Parallel Assignment
Primary outcome: Fasting insulin/glucose ratio
Secondary outcome: Number of subjects with above normal upper limit(s) of: insulin leveltestosterone low-density lipoprotein (LDL) cholesterol luteinizing hormone (LH)/follicle stimulating hormone (FSH) ratio dehydroepiandrosterone (DHEA)
Detailed description:
Sodium valproate is an established antiepileptic drug used against a broad range of seizure
types. Lamotrigine, a newer antiepileptic drug available since late 1980s, has a similar
range of action and is approved as first-line treatment for epilepsy in the United States and
many European countries as well as in Hong Kong. Recently, concern has been raised over the
association between valproate treatment and polycystic ovarian syndrome, a condition
characterised by multiple cysts in the ovaries in women and a range of hormonal and metabolic
disturbances. Cross-sectional studies from Finland suggest that up to 40% of women treated
with valproate have polycystic ovaries. Lamotrigine substitution for valproate has been
reported to normalise these parameters in some patients. Elevated serum insulin and androgen
levels have also been reported in over 50% of male patients taking valproate for epilepsy.
However, such high incidence of hormonal abnormalities associated with valproate treatment
has not been reproduced in studies conducted in other western populations. No similar studies
in Chinese patients have been reported. In addition, these cross-sectional studies suffer
from many potential confounding factors, such as previous treatment with other antiepileptic
drugs, variation in duration of treatment, thus limiting the ability to establish a causal
relationship.
This phase IV study aims to examine whether valproate treatment is associated with hormonal
abnormalities in Chinese epilepsy patients. Newly diagnosed patients will be randomised to
receive valproate or lamotrigine and their hormonal profiles measured prospectively for 12
months.
Eligibility
Minimum age: 15 Years.
Maximum age: 55 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- Patients aged between 15 and 55
- Ethnically Chinese
- Newly diagnosed epilepsy requiring antiepileptic drug treatment; or patients
previously treated with antiepileptic drugs but have withdrawn from medication for at
least 1 year, and now require resumption of antiepileptic drug therapy due to seizure
relapse.
Exclusion Criteria:
- Post-menopausal women.
- Pregnant women.
- Women who have undergone oophorectomy.
- Women taking or have taken oral contraceptive pills in the previous 3 months.
- Women diagnosed with or suspected to have polycystic ovarian syndrome.
- Subjects with diabetes mellitus.
- Subjects receiving hormone replacement or glucocorticoids.
- Subjects receiving long-term warfarin.
- Subjects suffering from significant systemic diseases, or illnesses that interfere
with pituitary-gonadal functions.
- Subjects with a progressive or degenerative neurological disorder.
- Subjects who are unable to take their medication reliably.
Locations and Contacts
Patrick Kwan, FHKAM, Phone: 852-2632-2211, Email: patrickkwan@cuhk.edu.hk
Prince of Wales Hospital, Shatin, Hong Kong; Recruiting Patrick Kwan, FHKAM, Phone: 852-2632-2211, Email: patrickkwan@cuhk.edu.hk Evelyn Yu, MSc, Phone: 852-2632-3856, Email: evelyn.yu@cuhk.edu.hk Patrick Kwan, FHKAM, Principal Investigator Howan Leung, MRCP, Sub-Investigator
United Christian Hospital, Kowloon, Hong Kong; Recruiting Ping Wing Ng, FHKAM Ping Wing Ng, FHKAM, Principal Investigator
Additional Information
Starting date: November 2004
Ending date: July 2008
Last updated: October 30, 2007
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