loperamide has been researched along with Leanness in 1 studies
Loperamide: One of the long-acting synthetic ANTIDIARRHEALS; it is not significantly absorbed from the gut, and has no effect on the adrenergic system or central nervous system, but may antagonize histamine and interfere with acetylcholine release locally.
loperamide : A synthetic piperidine derivative, effective against diarrhoea resulting from gastroenteritis or inflammatory bowel disease.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 1 (100.00) | 2.80 |
Authors | Studies |
---|---|
Richter, HE | 1 |
Jelovsek, JE | 1 |
Iyer, P | 1 |
Rogers, RG | 1 |
Meyer, I | 1 |
Newman, DK | 1 |
Bradley, MS | 1 |
Harm-Ernandes, I | 1 |
Dyer, KY | 1 |
Wohlrab, K | 1 |
Mazloomdoost, D | 1 |
Gantz, MG | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
Refractory Overactive Bladder: Sacral NEuromodulation v. BoTulinum Toxin Assessment (ROSETTA)[NCT01502956] | Phase 3 | 386 participants (Actual) | Interventional | 2012-02-29 | Completed | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
The primary outcome is the change from baseline in mean number of UUI episodes over the first 6-month visit period (1, 2, 3, 4, 5 and 6 month assessments); and is measured using 3-day bladder diaries administered monthly for the first 6 month visit period. (NCT01502956)
Timeframe: 6 Months
Intervention | UUI episodes (Mean) |
---|---|
InterStim® Device | -3.25 |
Botox® Injection | -3.89 |
Change from baseline in quality of life measures over the first 6 month visit period (6 month assessment) as measured by the Health Utility Index, Version 3 (HUI-3). The HUI 3 scale has a range from 0 to 1 with higher scores representing better health. (NCT01502956)
Timeframe: 6 Months
Intervention | units on a scale (Mean) |
---|---|
InterStim® Device | -0.006 |
Botox® Injection | -0.011 |
Change from baseline in quality of life measures over the first 6 month visit period (6 month assessment) as measured by the change in the mean Incontinence Impact Questionnaire short form (IIQ-SF) score. The IIQ-SF scale has a range from 0 to 100 with higher scores indicating a worse quality of life. (NCT01502956)
Timeframe: 6 Months
Intervention | units on a scale (Mean) |
---|---|
InterStim® Device | -10.4 |
Botox® Injection | -12.4 |
Change from baseline in quality of life measures over the first 6 month visit period (6 month assessment) as measured by the change in mean Urinary Distress Inventory Short Form (UDI-SF) score. The UDI-SF scale has a range from 0 to 100 with higher scores indicating greater distress. (NCT01502956)
Timeframe: 6 Months
Intervention | units on a scale (Mean) |
---|---|
InterStim® Device | -8.6 |
Botox® Injection | -10.0 |
"Treatment preference as measured by the Overactive Bladder Satisfaction of Treatment Questionnaire (OAB-SATq) at 6 months (6 month assessment).OAB-SATq treatment preference is a binary outcome that is classified as yes if a participant answers either Slight preference for the treatment I am receiving now or Definitely prefer the treatment I am receiving now to the question Do you prefer the treatment that you received since entering this study to the treatment you received before the study?" (NCT01502956)
Timeframe: 6 Months
Intervention | Participants (Count of Participants) |
---|---|
InterStim® Device | 89 |
Botox® Injection | 113 |
Change in mean Overactive Bladder Questionnaire Short Form (OABq-SF) score throughout baseline to the first 6-month visit (1, 2, 3, 4, 5, and 6-month assessments). Values range from 0 to 100 with higher scores on the symptom scale indicating greater severity of symptoms and higher scores on the quality of life scale indicating a better quality of life. (NCT01502956)
Timeframe: 6 Months
Intervention | units on a scale (Mean) | |
---|---|---|
OABq-SF Symptom Bother | OABq-SF Quality of Life | |
Botox® Injection | -46.7 | 41.6 |
InterStim® Device | -38.6 | 38.1 |
Proportion of subjects who report adequate improvement of their bladder function and urinary leakage with the Patient Global Impression of Improvement Questionnaire (PGI-I) at 6 months. Adequate improvement is defined as a rating of 1, 2, or 3 (better) on the patient-reported measure of perceived improvement with treatment on a scale of 1 (very much better) to 7 (very much worse). (NCT01502956)
Timeframe: 6 Months
Intervention | Participants (Count of Participants) | |
---|---|---|
Urinary leakage | Bladder function | |
Botox® Injection | 101 | 100 |
InterStim® Device | 91 | 92 |
Severity of urge incontinence symptoms at 6 month visit period as measured by the Sandvik questionnaire. The Sandvik score is a patient-reported measure of incontinence severity as assessed on a scale of slight (1-2), moderate (3-6), severe (8-9), very severe (12) to severe (10-12) using a standard scoring algorithm. (NCT01502956)
Timeframe: 6 Months
Intervention | Participants (Count of Participants) | |||
---|---|---|---|---|
Sandvik Slight | Sandvik Moderate | Sandvik Severe | Sandvik Very Severe | |
Botox® Injection | 29 | 33 | 28 | 36 |
InterStim® Device | 23 | 33 | 24 | 44 |
Treatment satisfaction as measured by the mean Overactive Bladder Satisfaction of Treatment Questionnaire (OAB-SATq) score at 6 months (6 month assessment). The OAB-SATq score ranges from 0 to 100 and includes 5 subscales: treatment satisfaction, side effects, treatment endorsement, convenience, and treatment preference, with higher scores reflecting better satisfaction. (NCT01502956)
Timeframe: 6 months
Intervention | units on a scale (Mean) | |||
---|---|---|---|---|
OAB-SATq Treatment Satisfaction | OAB-SATq Adverse Effects | OAB-SATq Endorsement | OAB-SATq Convenience | |
Botox® Injection | 67.7 | 88.4 | 78.1 | 67.6 |
InterStim® Device | 59.8 | 85.1 | 67.6 | 70.2 |
Change in mean number of urinary incontinence episodes (any type) and nocturia episodes from baseline over the first 6-month visit period (1, 2, 3, 4, 5, and 6-month assessments) as measured by the 3 day bladder diary. (NCT01502956)
Timeframe: 6 Months
Intervention | Number of episodes (Mean) | |
---|---|---|
Incontinence episodes (any) | Nocturia episodes | |
Botox® Injection | -4.02 | -0.40 |
InterStim® Device | -3.50 | -0.26 |
1 trial available for loperamide and Leanness
Article | Year |
---|---|
Characteristics Associated With Clinically Important Treatment Responses in Women Undergoing Nonsurgical Therapy for Fecal Incontinence.
Topics: Aged; Antidiarrheals; Biofeedback, Psychology; Combined Modality Therapy; Exercise Therapy; Fecal In | 2020 |