methylphenidate has been researched along with Weight Gain in 11 studies
Methylphenidate: A central nervous system stimulant used most commonly in the treatment of ATTENTION DEFICIT DISORDER in children and for NARCOLEPSY. Its mechanisms appear to be similar to those of DEXTROAMPHETAMINE. The d-isomer of this drug is referred to as DEXMETHYLPHENIDATE HYDROCHLORIDE.
methylphenidate : A racemate comprising equimolar amounts of the two threo isomers of methyl phenyl(piperidin-2-yl)acetate. A central stimulant and indirect-acting sympathomimetic, is used (generally as the hydrochloride salt) in the treatment of hyperactivity disorders in children and for the treatment of narcolepsy.
methyl phenyl(piperidin-2-yl)acetate : A amino acid ester that is methyl phenylacetate in which one of the hydrogens alpha to the carbonyl group is replaced by a piperidin-2-yl group.
Weight Gain: Increase in BODY WEIGHT over existing weight.
Excerpt | Relevance | Reference |
---|---|---|
" Although smoking cessation tends to result in weight increase, potentially initiating or exacerbating weight problems, adults with ADHD who are treated with osmotic release oral system methylphenidate (OROS-MPH) tend to lose weight." | 9.17 | Osmotic release oral system methylphenidate prevents weight gain during a smoking-cessation attempt in adults with ADHD. ( Heffner, JL; Lewis, DF; Winhusen, TM, 2013) |
" Although smoking cessation tends to result in weight increase, potentially initiating or exacerbating weight problems, adults with ADHD who are treated with osmotic release oral system methylphenidate (OROS-MPH) tend to lose weight." | 5.17 | Osmotic release oral system methylphenidate prevents weight gain during a smoking-cessation attempt in adults with ADHD. ( Heffner, JL; Lewis, DF; Winhusen, TM, 2013) |
"Four months after initiation of methylphenidate therapy the increased daytime sleepiness improved and excessive weight gain stopped." | 3.88 | Case report: narcolepsy type 1 in an adolescent with HIV infection-coincidence or potential trigger? ( Berger, C; Hackenberg, A; Paioni, P; Relly, C; Scherrer, KS, 2018) |
" A dose-response study was performed to monitor caloric intake, liquid intake and growth rate in rats following repeated administration of human oral therapeutic doses 2 mg/kg/day, 5mg/kg/day and 8mg/kg/day of methylphenidate." | 1.42 | Effect of repeated oral therapeutic doses of methylphenidate on food intake and growth rate in rats. ( Alam, N; Najam, R, 2015) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 2 (18.18) | 18.2507 |
2000's | 3 (27.27) | 29.6817 |
2010's | 5 (45.45) | 24.3611 |
2020's | 1 (9.09) | 2.80 |
Authors | Studies |
---|---|
Chirokikh, AA | 3 |
Uddin, SMZ | 3 |
Areikat, N | 3 |
Jones, R | 3 |
Duque, E | 3 |
Connor, C | 3 |
Hadjiargyrou, M | 3 |
Thanos, PK | 3 |
Komatsu, DE | 3 |
Scherrer, KS | 1 |
Relly, C | 1 |
Hackenberg, A | 1 |
Berger, C | 1 |
Paioni, P | 1 |
Benard, V | 1 |
Cottencin, O | 1 |
Guardia, D | 1 |
Vaiva, G | 1 |
Rolland, B | 1 |
Alam, N | 1 |
Najam, R | 1 |
Jahangard, L | 1 |
Akbarian, S | 1 |
Haghighi, M | 1 |
Ahmadpanah, M | 1 |
Keshavarzi, A | 1 |
Bajoghli, H | 1 |
Sadeghi Bahmani, D | 1 |
Holsboer-Trachsler, E | 1 |
Brand, S | 1 |
Heffner, JL | 1 |
Lewis, DF | 1 |
Winhusen, TM | 1 |
Achat-Mendes, C | 1 |
Anderson, KL | 1 |
Itzhak, Y | 1 |
Guerriero, RM | 1 |
Hayes, MM | 1 |
Dhaliwal, SK | 1 |
Ren, JQ | 1 |
Kosofsky, BE | 1 |
Poulton, A | 1 |
Schachar, RJ | 1 |
Tannock, R | 1 |
Cunningham, C | 1 |
Corkum, PV | 1 |
Schaller, JL | 1 |
Behar, D | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
A Pilot Study of Osmotic-Release Methylphenidate in Initiating and Maintaining Abstinence in Smokers With ADHD[NCT00253747] | Phase 3 | 255 participants (Actual) | Interventional | 2005-11-30 | Completed | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
A Generalized Estimating Equations(GEE)model which included treatment group, week, site, and treatment by week and site by week interaction effects was used to compare the groups on the DSM-IV ADHD total severity score (18 domains score at severity levels of 0[none]-3[severe]; maximum score 54) as measured at screening/baseline and study weeks 1-4 using the the interviewer-administered DSM-IV checklist and by the severity portion of the National Institute of Mental Health Clinical Global Impression (CGI) scale to rate the severity of the participant's ADHD symptoms. A single severity score ranging from 1 to 7 is yielded by the CGI severity scale. (NCT00253747)
Timeframe: Baseline and Study weeks 1,4,7,9,11
Intervention | DSM IV ADHD Score (Mean) |
---|---|
Osmotic-Release Methylphenidate (OROS-MPH)-Baseline | 38.4 |
Osmotic-Release Methylphenidate (OROS-MPH) - Placebo-Baseline | 36.6 |
Osmotic-Release Methylphenidate (OROS-MPH)-Week 11 | 16.4 |
Osmotic-Release Methylphenidate (OROS-MPH) - Placebo-Week 11 | 24.2 |
Release Methylphenidate (OROS-MPH)-Week 4 | 20.4 |
Osmotic-Release Methylphenidate (OROS-MPH) - Placebo-Week 4 | 27.2 |
Release Methylphenidate (OROS-MPH)-Week 7 | 20 |
Osmotic-Release Methylphenidate (OROS-MPH) - Placebo-Week 7 | 24 |
Release Methylphenidate (OROS-MPH)-Week 9 | 17.3 |
Methylphenidate (OROS-MPH) - Placebo-Week 9 | 23.9 |
A logistic regression including site and treatment group will be used to model rates of achieving point prevalence abstinence as assessed at the final visit of the O-MPH/P-Stnd Smoking Tx phase. Point prevalence abstinence was defined as not smoking in the previous seven days based on self-report using the TLFB method and confirmed with a Carbon Monoxide (CO) level <8 ppm. (NCT00253747)
Timeframe: Week 11
Intervention | participants (Number) |
---|---|
Osmotic-Release Methylphenidate (OROS-MPH) | 24 |
Osmotic-Release Methylphenidate (OROS-MPH) - Placebo | 26 |
"The smoking quit date was considered the first day of the O-MPH/P-Stnd Smoking Tx phase, which lasted for 6 weeks or more precisely 42 days (i.e., approximately weeks 5-10). The grace period was the first two weeks (i.e., days 1-14) with the remaining four weeks (days 15-42) comprising the period in which the participant must not meet criteria for treatment failure in order to be scored as obtaining prolonged abstinence. Self-report of cigarette use was assessed using a time-line follow-back (TLFB) assessment using carbon monoxide (CO)levels to correct self-reported smoking days. Smoking days were determined by starting with self-reported smoking and non-smoking days and using CO levels measured at weekly visits to modify the self-reports." (NCT00253747)
Timeframe: Weeks 7-10
Intervention | participants (Number) |
---|---|
Osmotic-Release Methylphenidate (OROS-MPH) | 25 |
Osmotic-Release Methylphenidate (OROS-MPH) - Placebo | 28 |
3 trials available for methylphenidate and Weight Gain
Article | Year |
---|---|
Children with ADHD and symptoms of oppositional defiant disorder improved in behavior when treated with methylphenidate and adjuvant risperidone, though weight gain was also observed - Results from a randomized, double-blind, placebo-controlled clinical t
Topics: Adjuvants, Pharmaceutic; Attention Deficit and Disruptive Behavior Disorders; Attention Deficit Diso | 2017 |
Osmotic release oral system methylphenidate prevents weight gain during a smoking-cessation attempt in adults with ADHD.
Topics: Administration, Oral; Adult; Attention Deficit Disorder with Hyperactivity; Female; Humans; Male; Me | 2013 |
Behavioral, situational, and temporal effects of treatment of ADHD with methylphenidate.
Topics: Affect; Attention Deficit Disorder with Hyperactivity; Central Nervous System Stimulants; Child; Chi | 1997 |
8 other studies available for methylphenidate and Weight Gain
Article | Year |
---|---|
Combined methylphenidate and fluoxetine treatment in adolescent rats significantly impairs weight gain with minimal effects on skeletal development.
Topics: Animals; Body Weight; Fluoxetine; Male; Methylphenidate; Rats; Rats, Sprague-Dawley; Weight Gain | 2023 |
Combined methylphenidate and fluoxetine treatment in adolescent rats significantly impairs weight gain with minimal effects on skeletal development.
Topics: Animals; Body Weight; Fluoxetine; Male; Methylphenidate; Rats; Rats, Sprague-Dawley; Weight Gain | 2023 |
Combined methylphenidate and fluoxetine treatment in adolescent rats significantly impairs weight gain with minimal effects on skeletal development.
Topics: Animals; Body Weight; Fluoxetine; Male; Methylphenidate; Rats; Rats, Sprague-Dawley; Weight Gain | 2023 |
Combined methylphenidate and fluoxetine treatment in adolescent rats significantly impairs weight gain with minimal effects on skeletal development.
Topics: Animals; Body Weight; Fluoxetine; Male; Methylphenidate; Rats; Rats, Sprague-Dawley; Weight Gain | 2023 |
Case report: narcolepsy type 1 in an adolescent with HIV infection-coincidence or potential trigger?
Topics: Adolescent; Central Nervous System Stimulants; Drug Monitoring; HIV Infections; Humans; Male; Methyl | 2018 |
The impact of discontinuing methylphenidate on weight and eating behavior.
Topics: Adolescent; Attention Deficit Disorder with Hyperactivity; Body Mass Index; Central Nervous System S | 2015 |
Effect of repeated oral therapeutic doses of methylphenidate on food intake and growth rate in rats.
Topics: Administration, Oral; Animals; Anxiety; Appetite Regulation; Behavior, Animal; Central Nervous Syste | 2015 |
Methylphenidate and MDMA adolescent exposure in mice: long-lasting consequences on cocaine-induced reward and psychomotor stimulation in adulthood.
Topics: Age Factors; Animals; Central Nervous System Stimulants; Cocaine; Conditioning, Psychological; Male; | 2003 |
Preadolescent methylphenidate versus cocaine treatment differ in the expression of cocaine-induced locomotor sensitization during adolescence and adulthood.
Topics: Age Factors; Analysis of Variance; Animals; Animals, Newborn; Behavior, Animal; Cocaine; Cocaine-Rel | 2006 |
Effect of long-term treatment with stimulant medication on growth?
Topics: Attention Deficit Disorder with Hyperactivity; Body Height; Body Weight; Central Nervous System Stim | 2007 |
Carbamazepine and methylphenidate in ADHD.
Topics: Adolescent; Attention Deficit Disorder with Hyperactivity; Carbamazepine; Drug Administration Schedu | 1999 |