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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00223262
Other study ID # LMC-R62
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date August 2002
Est. completion date September 2005

Study information

Verified date April 2019
Source University of Texas Southwestern Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine if lamotrigine therapy is associated with improvement in mood, memory and hippocampal size and function in patients receiving chronic corticosteroid therapy. Standard care for mood changes associated with corticosteroid therapy, if severe, includes antidepressants or other medications which can influence mood. No therapies, other than dose reduction or discontinuation, are currently available for memory loss associated with corticosteroid treatment. However, very little information is available on the treatment of either mood or memory changes associated with corticosteroid treatment, thus the proposed project may improve standard care.


Recruitment information / eligibility

Status Completed
Enrollment 28
Est. completion date September 2005
Est. primary completion date September 2005
Accepts healthy volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Current Corticosteroid Use of 7 mg or more for 6+ months

- 18-65 years of age

Exclusion Criteria:

- Primarily non-English speaking

- Pregnant/nursing woman

- Currently taking Depakote

- Currently taking Rifampin

- Has diagnosis of major depressive disorder, schizophrenia, PTSD, bipolar I or bipolar II (not related to corticosteroid use)

- Diseases with CNS involvement

- Is to start a brief steroid taper

- History of Alcohol/drug abuse/dependence

Study Design


Related Conditions & MeSH terms

  • Atrophy
  • Hippocampal Atrophy Due to Corticosteroid
  • Hypomania Due to Corticosteroid Use
  • Memory Impairment Due to Corticosteroid Use

Intervention

Drug:
Lamotrigine (Drug)


Locations

Country Name City State
United States The UT Southwestern Medical Center Dallas Texas

Sponsors (1)

Lead Sponsor Collaborator
University of Texas Southwestern Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Rey Auditory Verbal Learning Test (RAVLT) Rey Auditory Verbal Learning Test (RAVLT) is a test of verbal learning and declarative memory. During the test, 15 nouns that are read aloud for 5 consecutive trials. Each trial is followed by a free recall test (participant is asked to recall the words that were just read to them). The sum of correctly recalled words across 5 trials is called the total raw score. On completion of Trial 5, an interference list of 15 words (List B) is presented, followed by a free recall test of that list. After a 20-min delay, the examinee is again required to recall the words from list A - this is called the delay raw score. The raw scores on both the total recall and the delay trials (number of words correct across trials 1-5) are converted to standardized T-scores (Mean=50; SD=10; range 20-100) based on participant age and gender. The scores below are presented as T-scores, with higher scores indicative of better performance. 24 weeks