Last updated: 11/04/2018 08:49:51
An Open-Label Trial Measuring Satisfaction And Convenience Of Two Formulations Of Lamotrigine In Subjects With A Mood Disorder
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: An Open-Label Trial Measuring Satisfaction and Convenience of Two Formulations of Lamotrigine in Subjects with a Mood Disorder
Trial description: To determine the convenience and satisfaction of new orally disintegrating tablet formulation (ODT) of lamictal in subjects with a mood disorder. This was a multicenter, open-label study in participants with a mood disorder, who reported difficulty or discomfort in swallowing the currently marketed IR compressed tablet formulation of lamotrigine and who had a person (such as a spouse, partner, companion, aid, nurse, caregiver, etc) willing to complete a Companion/Caregiver Question. Subjects were switched from the currently marketed lamotrigine IR formulation to a matching dose of lamotrigine IR orally disintegrating tablet (ODT) for 3 weeks to determine convenience and satisfaction.
Primary purpose:
Treatment
Trial design:
Single Group Assignment
Masking:
None (Open Label)
Allocation:
Non-randomized
Primary outcomes:
Mean change from baseline in the Convenience Subscale Score (CSS) derived from the Treatment Satisfaction Questionnaire for Medication (TSQM v 1.4) using items 9 (ease of use), 10 (ease of planning to use), and 11 (convenience) at Week 3.
Timeframe: Baseline, End of Study (Week 3) or Early Withdrawal
Secondary outcomes:
Mean change from baseline in the Global Satisfaction Subscale Score, from the TSQM using items 12 (confidence in medicine), 13 (certainty that good things about medication outweigh bad things), and 14 (satisfaction with medication) at Week 3
Timeframe: Baseline, End of Study (Week 3) or Early Withdrawal
Mean change from baseline in Clinical Global Impression of Illness-Severity at Week 3
Timeframe: Baseline, End of Study (Week 3) or at Early Withdrawal
Mean change from baseline in the Beck Depression Inventory (BDI-II) score at Week 3
Timeframe: Baseline, End of Study (Week 3 weeks) or at Early Withdrawal
Number of participants answering the question "Did the tablets dissolve instantly (yes or no)?" at Week 3
Timeframe: End of Study (Week 3) or Early Withdrawal
Number of participants answering the question "How satisfied or dissatisfied were you with the time it took the tablet to dissolve" at Week 3
Timeframe: Baseline, End of Study (Week 3) or Early Withdrawal
Number of participants answering the question “How did the dissolved tablet feel in your mouth?” at Week 3
Timeframe: End of Study (Week 3) or Early Withdrawal
Number of participants answering the question "How satisfied were you with the flavor of the tablet?" at Week 3
Timeframe: End of Study (Week 3) or Early Withdrawal
Number of participants answering the question "How would you rate the strength of the flavor of the tablet"? at Week 3
Timeframe: End of Study (Week 3) or Early Withdrawal
Number of participants answering the question "How would you rate the aftertaste of the tablet"? at Week 3.
Timeframe: End of Study (Week 3) or Early Withdrawal
Number of participants answering the question "How satisfied were you with the aftertaste of the tablet"? at Week 3
Timeframe: Baseline, End of Study (Week 3) or Early Withdrawal
Number of participants answering the question "Compared to standard tablets that need to be swallowed with liquid, how convenient or inconvenient did you find this orally disintegrating tablet"? at Week 3
Timeframe: End of Study (Week 3) or at Early Withdrawal
Number of participants answering the question "Compared to standard tablets that need to be swallowed with liquid, how easy or difficult is it to use this orally disintegrating tablet?" at Week 3
Timeframe: End of Study (Week 3) or at Early Withdrawal
Number of participants indicating a preference for ODT or the standard IR tablet at Week 3
Timeframe: End of Study (Week 3) or at Early Withdrawal
Number of companions/caregivers indicating whether ODT or standard IR tablet is more convenient at Week 3
Timeframe: End of Study (Week 3) or at Early Withdrawal
Number of participants indicating at Week 3 (by answering yes/no) that they would be more likely to take the ODT formulation
Timeframe: End of Study (Week 3) or at Early Withdrawal
Interventions:
Enrollment:
97
Primary completion date:
2008-20-02
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
Martha Sajatovic; Thomas R Thompson; Kevin Nanry; Suzanne Edwards . A Prospective, Open-Label Trial Measuring Satisfaction and Convenience of Two Formulations of Lamotrigine in Subjects with Mood Disorders . Patient Prefer Adherence. 2013;7:411-417.
Medical condition
Mood Disorders
Product
lamotrigine
Collaborators
Not applicable
Study date(s)
January 2008 to February 2008
Type
Interventional
Phase
3
Participation criteria
Sex
Female & Male
Age
18+ years
Accepts healthy volunteers
No
- Subject must have a documented diagnosis of a mood disorder as defined by Diagnostic and Statistical Manual of Mental Disorders (DSM)-IV (296.00-296.90).
- Subject must have a person (such as a spouse, partner, companion, aid, nurse, caregiver, etc) willing to complete a Companion/Caregiver Preference Question either in person or via the telephone. This individual must read, write, and comprehend English at a level sufficient to complete study-related assessments.
- Subject has:
- a current (or within six months prior to Screening) diagnosis of anorexia nervosa or bulimia.
Inclusion and exclusion criteria
Inclusion criteria:
- Subject must have a documented diagnosis of a mood disorder as defined by Diagnostic and Statistical Manual of Mental Disorders (DSM)-IV (296.00-296.90).
- Subject must have a person (such as a spouse, partner, companion, aid, nurse, caregiver, etc) willing to complete a Companion/Caregiver Preference Question either in person or via the telephone. This individual must read, write, and comprehend English at a level sufficient to complete study-related assessments.
- Subject must have been taking a stable dose of currently marketed compressed tablet formulation of lamotrigine IR for at least 4 weeks prior to Baseline (Day 1) of the study and must be adherent to the prescribed dosing regimen. The current dose must not exceed 600 mg/day.
- Subject's current lamotrigine IR dose, frequency and number of tablets per administration must remain consistent between the IR and ODT regimens. However, the subject's current lamotrigine IR dose may be such that the subject would receive no more than one additional ODT per administration in order to equal their IR dose.
- Subject must currently report a difficulty or discomfort swallowing lamotrigine IR compressed tablets, the nature of which is or will be documented. NOTE: A diagnosis of dysphagia is not required.
- Subject must have the ability to comprehend the consent form and provide informed consent.
- Subject must read, write, and comprehend English at a level sufficient to complete study-related assessments.
- Subject is a male or female at least 18 years of age.
- If female, the subject is eligible to enter and participate in this study if she is not lactating and is of: a.non-childbearing potential (i.e., physiologically incapable of becoming pregnant, including any female who is pre-menarchal or post-menopausal [defined as one year without menses]); is surgically sterile [via hysterectomy and/or removal of the ovaries] or, b.child-bearing potential, has a negative pregnancy test at both Screening and/or Baseline (prior to Investigational Product administration), and agrees to one of the following requirements:
- has a male sexual partner who is surgically sterilized (vasectomy with documentation of azoospermia) prior to Screening or,
- sexual partner(s) is/are exclusively female or,
- double barrier method: condom or occlusive cap (diaphragm or cervical/vault caps) plus spermicidal agent (foam/gel/film/cream/suppository). The subject must be using this method for at least 1 week following the discontinuation of Investigational Product or,
- any intrauterine device (IUD) with published data showing that the highest expected failure rate is less than 1% per year. Acceptable IUDs, for the purposes of this study, include TCu-380A (Paragard), TCU-380 Slimline (Gyne T Slimline), MULTILOAD-250 (MLCu-250) and 375, Levonorgesterol LNG-20 Intrauterine System (Mirena/Levonova), and Flexigard 330/CuFix PP330 (Gynefix).The subject must have had the device inserted at least 2 weeks prior to Screening, throughout the study, and 2 weeks following the discontinuation of Investigational Product.
Exclusion criteria:
- Subject has:
- a current (or within six months prior to Screening) diagnosis of anorexia nervosa or bulimia.
- a diagnosis of a mood disorder due to a general medical condition, or substance abuse per DSM-IV (293.83).
- a diagnosis of schizophrenia or other psychotic disorders.
- Subject who meets current criteria of an acute mood disorder and has a CGI-S of ≥4 at Screening.
- Subject who crushes lamotrigine IR compressed tablet prior to taking or receiving medication orally.
- Subject who, in the investigator's judgment, poses a homicidal or serious suicidal risk; has made a suicide attempt within the six months preceding Screening; or has ever been homicidal.
- Subject who has a score of 1 or greater on Suicidality item (Item 9) of the BDI-II at Screening and/or Baseline.
- Subject has ever experienced a rash related to prior lamotrigine treatment, or for whom treatment was discontinued for clinically significant safety reasons.
- Subject has a history of severe hepato-biliary disease within the past 3 years.
- Subject has any medical condition that, in the investigator's judgment, is considered to be clinically significant and could potentially affect subject safety or study outcome.
- Subject has a positive urine test at Screening for illicit drug use and/or a history of alcohol or substance abuse or dependence within the past 12 months.
- Subject is currently participating in another clinical study in which the subject is or will be exposed to an investigational or non-investigational drug or device, or has done so within the preceding month for studies unrelated to the current illness, or six months for studies related to the current illness.
- Female subject is pregnant, lactating, or does not agree to use contraceptive method(s) specified in the protocol to avoid pregnancy during the study.
Trial location(s)
Location
GSK Investigational Site
Norfolk, Virginia, United States, 23505
Status
Study Complete
Location
GSK Investigational Site
Raleigh, North Carolina, United States, 27609
Status
Study Complete
Location
GSK Investigational Site
Fairview Heights, Illinois, United States, 62208
Status
Study Complete
Location
GSK Investigational Site
Santa Ana, California, United States, 92705
Status
Study Complete
Location
GSK Investigational Site
Winter Park, Florida, United States, 32792
Status
Study Complete
Showing 1 - 6 of 18 Results
Study documents
Clinical study report
Available language(s): English
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Results posted on ClinicalTrials.gov
Recruitment status
Study complete
Actual primary completion date
2008-20-02
Actual study completion date
2008-20-02
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
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