rabeprazole has been researched along with Body Weight in 6 studies
Rabeprazole: A 4-(3-methoxypropoxy)-3-methylpyridinyl derivative of timoprazole that is used in the therapy of STOMACH ULCERS and ZOLLINGER-ELLISON SYNDROME. The drug inhibits H(+)-K(+)-EXCHANGING ATPASE which is found in GASTRIC PARIETAL CELLS.
Body Weight: The mass or quantity of heaviness of an individual. It is expressed by units of pounds or kilograms.
Excerpt | Relevance | Reference |
---|---|---|
"Evaluate the efficacy and safety of rabeprazole in children, 1 to 11 years old, with endoscopically/histologically proven gastroesophageal reflux disease (GERD)." | 9.17 | Efficacy and safety of rabeprazole in children (1-11 years) with gastroesophageal reflux disease. ( Haddad, I; Hu, P; Kierkus, J; Leitz, G; Silber, S; Sloan, S; Tron, E; Ulmer, A, 2013) |
"The pharmacokinetics of rabeprazole after a single oral dose and once-daily administration for 5 consecutive days was characterized in children 1 to 11 years old with gastroesophageal reflux disease (GERD)." | 9.15 | Pharmacokinetics and tolerability of rabeprazole in children 1 to 11 years old with gastroesophageal reflux disease. ( Doose, DR; Gonzalez, MD; Haddad, I; Leitz, GJ; Mulberg, AE; Rusch, S; Solanki, B; Zannikos, PN, 2011) |
": The efficacy and safety of rabeprazole, a proton pump inhibitor, were studied in infants with gastroesophageal reflux disease (GERD)." | 5.19 | Safety and efficacy of delayed release rabeprazole in 1- to 11-month-old infants with symptomatic GERD. ( Hoffman, D; Hu, P; Hussain, S; Kierkus, J; Lekich, R; Sloan, S; Treem, W, 2014) |
"Evaluate the efficacy and safety of rabeprazole in children, 1 to 11 years old, with endoscopically/histologically proven gastroesophageal reflux disease (GERD)." | 5.17 | Efficacy and safety of rabeprazole in children (1-11 years) with gastroesophageal reflux disease. ( Haddad, I; Hu, P; Kierkus, J; Leitz, G; Silber, S; Sloan, S; Tron, E; Ulmer, A, 2013) |
"The pharmacokinetics of rabeprazole after a single oral dose and once-daily administration for 5 consecutive days was characterized in children 1 to 11 years old with gastroesophageal reflux disease (GERD)." | 5.15 | Pharmacokinetics and tolerability of rabeprazole in children 1 to 11 years old with gastroesophageal reflux disease. ( Doose, DR; Gonzalez, MD; Haddad, I; Leitz, GJ; Mulberg, AE; Rusch, S; Solanki, B; Zannikos, PN, 2011) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (16.67) | 29.6817 |
2010's | 5 (83.33) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Haddad, I | 2 |
Kierkus, J | 2 |
Tron, E | 1 |
Ulmer, A | 1 |
Hu, P | 2 |
Sloan, S | 2 |
Silber, S | 1 |
Leitz, G | 1 |
Hussain, S | 1 |
Hoffman, D | 1 |
Lekich, R | 1 |
Treem, W | 1 |
Kimko, H | 1 |
Thyssen, A | 1 |
Mould, DR | 1 |
Mannaert, E | 1 |
Treem, WR | 1 |
Yasu, T | 1 |
Konuma, T | 1 |
Kato, S | 1 |
Kurokawa, Y | 1 |
Takahashi, S | 1 |
Tojo, A | 1 |
Yoshikawa, I | 1 |
Nagato, M | 1 |
Yamasaki, M | 1 |
Kume, K | 1 |
Otsuki, M | 1 |
Zannikos, PN | 1 |
Doose, DR | 1 |
Leitz, GJ | 1 |
Rusch, S | 1 |
Gonzalez, MD | 1 |
Solanki, B | 1 |
Mulberg, AE | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
A Multi-Center, Double-Blind, Parallel-Group Study to Evaluate Short-term Safety and Efficacy and Long-Term Maintenance of Two Dose Levels of Rabeprazole Sodium Delayed-Release Pediatric Bead Formulation in 1- to 11-Year Old Pediatric Subjects With Endosc[NCT00787891] | Phase 3 | 127 participants (Actual) | Interventional | 2009-01-31 | Completed | ||
A Multi-Center, Double-Blind, Randomized, Placebo-Controlled, Parallel Group, Withdrawal Study to Evaluate the Safety and Efficacy of Delayed Release Rabeprazole in 1- to 11-Month-Old Pediatric Subjects With Symptomatic/Gastroesophageal Erosive Reflux Dis[NCT00992589] | Phase 3 | 344 participants (Actual) | Interventional | 2009-11-30 | Completed | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
The Hetzel and Dent Classification grades range from 0 (normal esophageal mucosa, no abnormalities noted) to 4 (deep ulcers anywhere in the esophagus or ulceration of more than half of the esophageal mucosa). Higher observed scores indicate more serious condition. For change of baseline, a score of 0 indicates no change; a positive score indicates the condition is worsening, while a negative score indicates an improvement. (NCT00787891)
Timeframe: Baseline, Week 36
Intervention | Scores on a scale (Mean) |
---|---|
Rabeprazole Sodium 0.5 mg/kg | 0.2 |
Rabeprazole Sodium 1.0 mg/kg | 0.2 |
The Hetzel and Dent Classification grades range from 0 (normal esophageal mucosa, no abnormalities noted) to 4 (deep ulcers anywhere in the esophagus or ulceration of more than half of the esophageal mucosa). Higher observed scores indicate more serious condition. For change of baseline, a score of 0 indicates no change; a positive score indicates the condition is worsening, while a negative score indicates an improvement. (NCT00787891)
Timeframe: Baseline, Week 12
Intervention | Scores on a scale (Mean) |
---|---|
Rabeprazole Sodium 0.5 mg/kg | -1.3 |
Rabeprazole Sodium 1.0 mg/kg | -1.0 |
The gastroesophageal reflux disease (GERD) symptom and severity scale measures the frequency (0= Never; 1= 1-2 times; 2= 3-4 times; 3= 5-6 times; 4= 7 or more times) and the severity (1= Mild; 2= Moderate; 3=Severe) of GERD symptoms. The score is defined as the sum of the frequency (0-4) and severity (1-3) of that symptom. The total score is the sum of the scores of all the symptoms and ranges from 12 to 84. Higher scores indicate more serious condition. For change from baseline, 0 indicates no change; a positive score indicates worsening, while a negative score indicates improvement. (NCT00787891)
Timeframe: Baseline, Week 36
Intervention | Scores on a scale (Mean) |
---|---|
Rabeprazole Sodium 0.5 mg/kg | -2.9 |
Rabeprazole Sodium 1.0 mg/kg | -1.4 |
The gastroesophageal reflux disease (GERD) symptom and severity scale measures the frequency (0= Never; 1= 1-2 times; 2= 3-4 times; 3= 5-6 times; 4= 7 or more times) and the severity (1= Mild; 2= Moderate; 3=Severe) of GERD symptoms. The score is defined as the sum of the frequency (0-4) and severity (1-3) of that symptom. The total score is the sum of the scores of all the symptoms and ranges from 12 to 84. Higher scores indicate more serious condition. For change from baseline, 0 indicates no change; a positive score indicates worsening, while a negative score indicates improvement. (NCT00787891)
Timeframe: Baseline, Week 12
Intervention | Scores on a scale (Mean) |
---|---|
Rabeprazole Sodium 0.5 mg/kg | -11.5 |
Rabeprazole Sodium 1.0 mg/kg | -8.5 |
Healing is defined as macroscopically normal esophageal mucosa or histologic normal esophageal mucosa. (NCT00787891)
Timeframe: 12 weeks
Intervention | Percentage of participants (Number) |
---|---|
Rabeprazole Sodium 0.5 mg/kg | 78 |
Rabeprazole Sodium 1.0 mg/kg | 83 |
Healing is defined as macroscopically normal esophageal mucosa or histologic normal esophageal mucosa. (NCT00787891)
Timeframe: 36 weeks
Intervention | Percentage of patients (Number) |
---|---|
Rabeprazole Sodium 0.5 mg/kg | 92 |
Rabeprazole Sodium 1.0 mg/kg | 88 |
(NCT00992589)
Timeframe: Baseline, Week 8
Intervention | frequency of Regurgitation (Mean) |
---|---|
Double-Blind Placebo | -0.8 |
Double-Blind Rabeprazole Sodium 5 mg | -0.8 |
Double-Blind Rabeprazole Sodium 10 mg | -1.6 |
Double-Blind Rabeprazole Sodium Total | -1.2 |
The Infant Gastroesophageal Reflux Questionnaire-Revised (I-GERQ-R) is a 12-item questionnaire that is completed by the primary caregiver at every office or telephonic visit. It has a weekly recall and the items cover the frequency, amount and discomfort attributed to spit-up, refusal or stopping feeding, crying and fussing, hiccups, arching back and stopping breathing or changing color. The total score is calculated as the sum of all 12 scores for the individual questions, and ranges from 0 to 42. A higher value indicates a worse outcome. (NCT00992589)
Timeframe: Baseline, Week 8
Intervention | scores on a scale (Mean) |
---|---|
Double-Blind Placebo | -3.6 |
Double-Blind Rabeprazole Sodium 5 mg | -3.8 |
Double-Blind Rabeprazole Sodium 10 mg | -4.1 |
Double-Blind Rabeprazole Sodium Total | -3.9 |
The Infant Gastroesophageal Reflux Questionnaire-Daily Diary (I-GERQ-DD) is a 9-item daily diary that the primary caregiver will be instructed to complete every evening at the same time interval after the participant has gone to sleep for the night. The I-GERQ-DD contains 3 subscales: the Regurgitation subscale, the Eating Behavior subscale and the Discomfort subscale. Each of the 9 items will be assigned a numeric score. The total score will be calculated as the sum of all 9 items, and ranges from 0 to 37. A higher value indicates a worse outcome. (NCT00992589)
Timeframe: Baseline, Week 8
Intervention | scores on a scale (Mean) |
---|---|
Double-Blind Placebo | -1.9 |
Double-Blind Rabeprazole Sodium 5 mg | -1.6 |
Double-Blind Rabeprazole Sodium 10 mg | -2.1 |
Double-Blind Rabeprazole Sodium Total | -1.9 |
The Infant Gastroesophageal Reflux Questionnaire-Daily Diary (I-GERQ-DD) is a 9-item daily diary that the primary caregiver will be instructed to complete every evening at the same time interval after the subject has gone to sleep for the night. The I-GERQ-DD contains 3 subscales: the Regurgitation subscale, the Eating Behavior subscale and the Discomfort subscale. The Discomfort subscale score will be calculated as the sum of the 3 questions regarding discomfort (Questions, 7, 8, 9) and will range from 0 to 12. For each subscale score, a higher value indicates a worse outcome. (NCT00992589)
Timeframe: Baseline, Week 8
Intervention | scores on a scale (Mean) |
---|---|
Double-Blind Placebo | 0.0 |
Double-Blind Rabeprazole Sodium 5 mg | -0.1 |
Double-Blind Rabeprazole Sodium 10 mg | -0.4 |
Double-Blind Rabeprazole Sodium Total | -0.2 |
The Infant Gastroesophageal Reflux Questionnaire-Daily Diary (I-GERQ-DD) is a 9-item daily diary that the primary caregiver will be instructed to complete every evening at the same time interval after the subject has gone to sleep for the night. The I-GERQ-DD contains 3 subscales: the Regurgitation subscale, the Eating Behavior subscale and the Discomfort subscale. The Eating Behavior subscale score will be calculated as the sum of the 3 questions regarding eating behavior (Questions 4, 5, 6) and will range from 0 to 12. For each subscale score, a higher value indicates a worse outcome. (NCT00992589)
Timeframe: Baseline, Week 8
Intervention | scores on a scale (Mean) |
---|---|
Double-Blind Placebo | -0.1 |
Double-Blind Rabeprazole Sodium 5 mg | -0.1 |
Double-Blind Rabeprazole Sodium 10 mg | -0.4 |
Double-Blind Rabeprazole Sodium Total | -0.3 |
The Infant Gastroesophageal Reflux Questionnaire-Daily Diary (I-GERQ-DD) is a 9-item daily diary that the primary caregiver will be instructed to complete every evening at the same time interval after the participant has gone to sleep for the night. The I-GERQ-DD contains 3 subscales: the Regurgitation subscale, the Eating Behavior subscale and the Discomfort subscale. The Regurgitation subscale will be calculated as the sum of the 3 questions regarding regurgitation (Questions 1, 2, 3) and will range from 0 to 13. For each subscale score, a higher value indicates a worse outcome. (NCT00992589)
Timeframe: Baseline, Week 8
Intervention | scores on a scale (Mean) |
---|---|
Double-Blind Placebo | -0.8 |
Double-Blind Rabeprazole Sodium 5 mg | -0.8 |
Double-Blind Rabeprazole Sodium 10 mg | -1.0 |
Double-Blind Rabeprazole Sodium Total | -0.9 |
Body weight was measured with the participant unclothed and before a feeding during each office visit. In the analysis of weight data, weight will be transformed to the weight-for-age Z-score using World Health Organization Child Growth Standards, taking into account the infant's age and gender (Borghi E, 2006). (NCT00992589)
Timeframe: Baseline, Week 8
Intervention | Z-score (Mean) |
---|---|
Double-Blind Placebo | 0.11 |
Double-Blind Rabeprazole Sodium 5 mg | 0.16 |
Double-Blind Rabeprazole Sodium 10 mg | 0.11 |
Double-Blind Rabeprazole Sodium Total | 0.14 |
(NCT00992589)
Timeframe: Baseline, Week 8
Intervention | number of episodes (Mean) | ||||
---|---|---|---|---|---|
Less than 1 tablespoon | 1 to 2 tablespoons | More than 2 tablespoons to 2 fluid oz | More than 2 fluid oz to 4 fluid oz | More than 4 fluid oz | |
Double-Blind Placebo - Baseline | 1.2 | 0.7 | 0.3 | 0.1 | 0.0 |
Double-Blind Placebo - Week 8 | 0.8 | 0.5 | 0.2 | 0.0 | 0.0 |
Double-Blind Rabeprazole Sodium 10 mg - Baseline | 1.9 | 1.2 | 0.3 | 0.0 | 0.0 |
Double-Blind Rabeprazole Sodium 10 mg - Week 8 | 1.0 | 0.7 | 0.2 | 0.0 | 0.0 |
Double-Blind Rabeprazole Sodium 5 mg - Baseline | 1.1 | 0.7 | 0.2 | 0.0 | 0.0 |
Double-Blind Rabeprazole Sodium 5 mg - Week 8 | 0.7 | 0.4 | 0.1 | 0.0 | 0.0 |
Double-Blind Rabeprazole Sodium Total - Baseline | 1.5 | 1.0 | 0.2 | 0.0 | 0.0 |
Double-Blind Rabeprazole Sodium Total - Week 8 | 0.9 | 0.6 | 0.2 | 0.0 | 0.0 |
3 trials available for rabeprazole and Body Weight
Article | Year |
---|---|
Efficacy and safety of rabeprazole in children (1-11 years) with gastroesophageal reflux disease.
Topics: Abdominal Pain; Body Weight; Child; Child, Preschool; Diarrhea; Dose-Response Relationship, Drug; Es | 2013 |
Safety and efficacy of delayed release rabeprazole in 1- to 11-month-old infants with symptomatic GERD.
Topics: Body Weight; Double-Blind Method; Gastroesophageal Reflux; Humans; Infant; Infant, Newborn; Male; Pr | 2014 |
Pharmacokinetics and tolerability of rabeprazole in children 1 to 11 years old with gastroesophageal reflux disease.
Topics: 2-Pyridinylmethylsulfinylbenzimidazoles; Age Factors; Area Under Curve; Body Weight; Child; Child, P | 2011 |
3 other studies available for rabeprazole and Body Weight
Article | Year |
---|---|
Helicobacter pylori treatment in children: defining a dose for rabeprazole as a part of a triple therapy regimen.
Topics: Adolescent; Amoxicillin; Area Under Curve; Body Weight; Child; Child, Preschool; Clarithromycin; Cli | 2015 |
Different effects of lansoprazole and rabeprazole on the plasma voriconazole trough levels in allogeneic hematopoietic cell transplant recipients.
Topics: Administration, Oral; Adolescent; Adult; Aged; Antifungal Agents; Body Weight; Bone Marrow Transplan | 2016 |
Long-term treatment with proton pump inhibitor is associated with undesired weight gain.
Topics: 2-Pyridinylmethylsulfinylbenzimidazoles; Aged; Blood Pressure; Body Mass Index; Body Weight; Case-Co | 2009 |