Page last updated: 2024-10-30

loperamide and Leanness

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.

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's1 (100.00)2.80

Authors

AuthorsStudies
Richter, HE1
Jelovsek, JE1
Iyer, P1
Rogers, RG1
Meyer, I1
Newman, DK1
Bradley, MS1
Harm-Ernandes, I1
Dyer, KY1
Wohlrab, K1
Mazloomdoost, D1
Gantz, MG1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Refractory Overactive Bladder: Sacral NEuromodulation v. BoTulinum Toxin Assessment (ROSETTA)[NCT01502956]Phase 3386 participants (Actual)Interventional2012-02-29Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

Number of Urge Urinary Incontinence (UUI) Episodes

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

InterventionUUI episodes (Mean)
InterStim® Device-3.25
Botox® Injection-3.89

Quality of Life (HUI-3)

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

Interventionunits on a scale (Mean)
InterStim® Device-0.006
Botox® Injection-0.011

Quality of Life (IIQ-SF)

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

Interventionunits on a scale (Mean)
InterStim® Device-10.4
Botox® Injection-12.4

Quality of Life (UDI-SF)

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

Interventionunits on a scale (Mean)
InterStim® Device-8.6
Botox® Injection-10.0

Treatment Satisfaction (OAB-SATq Treatment Preference)

"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

InterventionParticipants (Count of Participants)
InterStim® Device89
Botox® Injection113

Change in Overactive Bladder

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

,
Interventionunits on a scale (Mean)
OABq-SF Symptom BotherOABq-SF Quality of Life
Botox® Injection-46.741.6
InterStim® Device-38.638.1

Number of Participants With Improvement of Bladder Function and Urinary Leakage

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

,
InterventionParticipants (Count of Participants)
Urinary leakageBladder function
Botox® Injection101100
InterStim® Device9192

Severity of Urge Incontinence Symptoms

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

,
InterventionParticipants (Count of Participants)
Sandvik SlightSandvik ModerateSandvik SevereSandvik Very Severe
Botox® Injection29332836
InterStim® Device23332444

Treatment Satisfaction (OAB-SATq Treatment Satisfaction, Adverse Effects, Treatment Endorsement, and Convenience)

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

,
Interventionunits on a scale (Mean)
OAB-SATq Treatment SatisfactionOAB-SATq Adverse EffectsOAB-SATq EndorsementOAB-SATq Convenience
Botox® Injection67.788.478.167.6
InterStim® Device59.885.167.670.2

Urinary Frequency and Nocturia

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

,
InterventionNumber of episodes (Mean)
Incontinence episodes (any)Nocturia episodes
Botox® Injection-4.02-0.40
InterStim® Device-3.50-0.26

Trials

1 trial available for loperamide and Leanness

ArticleYear
Characteristics Associated With Clinically Important Treatment Responses in Women Undergoing Nonsurgical Therapy for Fecal Incontinence.
    The American journal of gastroenterology, 2020, Volume: 115, Issue:1

    Topics: Aged; Antidiarrheals; Biofeedback, Psychology; Combined Modality Therapy; Exercise Therapy; Fecal In

2020