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226 studies found for:    Open Studies | "Urination Disorders"
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Rank Status Study
21 Recruiting When is the Best Moment to Remove the Urinary Catheter After Laparoscopic Hysterectomy?
Conditions: Urinary Tract Infection;   Bladder Retention
Intervention: Device: Foley catheter
22 Recruiting The European Study of Altis Single Incision Sling System for Female Stress Urinary Incontinence
Condition: Stress Urinary Incontinence
Intervention: Device: Altis Single Incision Sling System
23 Recruiting Vaginal Estrogen for Asymptomatic Microscopic Hematuria
Condition: Asymptomatic Microscopic Hematuria
Intervention: Drug: Estradiol Ring
24 Recruiting Effect of Oral Supplementation With Curcumin in Patients With Proteinuric Diabetic Kidney Disease
Condition: Proteinuria
Interventions: Dietary Supplement: Curcumin;   Other: Placebo
25 Not yet recruiting Mirabegron for the Treatment of Pain Motivated Urinary Frequency and Urgency in Women
Conditions: Urinary Frequency/Urgency;   Bladder Irritable;   Bladder Pain Syndrome
Intervention: Drug: Mirabegron
26 Recruiting Availability Study of ACTH to Treat Children SRNS/SDNS
Condition: Proteinuria
Intervention: Drug: ACTH
27 Recruiting Shock Wave Lithotripsy Versus Visual Cystolitholapaxy in The Management of Patients Presenting With Calcular Acute Urinary Retention: A Randomized Controlled Trial.
Condition: Urinary Calculi
Interventions: Procedure: ESWL;   Procedure: Endoscopic treatment
28 Recruiting A Crossover Pilot Study of the Effect of Amiloride on Proteinuria
Condition: Proteinuria
Interventions: Drug: Amiloride;   Drug: Triamterene
29 Recruiting Belatacept Conversion in Proteinuric Kidney Transplant Recipients
Condition: Proteinuria
Intervention: Drug: Belatacept
30 Not yet recruiting An Investigation Into the Cardiovascular Risk and Aetiology of CKDu in Sri Lanka
Conditions: CKDu;   Arterial Stiffness;   Proteinuria;   Serum Creatinine;   Urinary Biomarkers;   DNA Adducts
Intervention: Device: Arterial Stiffness Assessment
31 Recruiting Effect of Vaginal Estrogen on Asymptomatic Microhematuria (AMH)
Condition: Microscopic Hematuria
Interventions: Drug: Premarin vaginal estrogen cream;   Drug: Placebo vaginal cream
32 Recruiting Proteinuria in Pre and Post Transplant
Condition: Proteinuria
Intervention:
33 Recruiting Determination of Kidney Function
Conditions: Kidney Disease;   Proteinuria;   Autoimmune / Connective Tissue Diseases
Intervention:
34 Recruiting Study to Assess Duration of Indwelling Catheter After Sacrocolpopexy
Conditions: Pelvic Organ Prolapse;   Urinary Tract Infections;   Urinary Retention
Interventions: Procedure: Immediate catheter removal;   Procedure: Post op day 1 catheter removal
35 Recruiting Comparative Study of PDVF and Polypropylene Transobturator Suburethral Tapes
Condition: Urinary Stress Incontinence
Interventions: Device: PVDF transobturator tape;   Device: Polypropylene transobturator tape
36 Recruiting Prostate Embolization for Acute Urinary Retention Study
Condition: Prostatic Hypertrophy, Benign
Intervention: Device: Bead Block
37 Recruiting Pharmacokinetics and Pharmacodynamics of Desmopressin Oral Lyophilisate Formulation in the Paediatric Population
Condition: Monosymptomatic Nocturnal Enuresis
Intervention: Drug: desmopressin
38 Recruiting Effect of Ambulatory BP Monitoring on the CliniCal coUrse and RenAl ouTcomE of CKD
Conditions: Chronic Kidney Diseases;   Renal Insufficiency, Chronic;   Albuminuria;   Hypertension
Intervention: Device: Ambulatory blood pressure monitoring (ABPM)
39 Recruiting Trial Investigating the Long Term Safety and Tolerability of Desmopressin Orally Disintegrating Tablets (ODT) for Nocturia Due to Nocturnal Polyuria in Japanese Subjects
Condition: Nocturia
Interventions: Drug: Desmopressin ODT 25 μg;   Drug: Desmopressin ODT 50 μg
40 Not yet recruiting Preoperative Administration of Tamsulosin for Prevention of Post Operative Urinary Retention in Males Undergoing Elective Inguinal Hernia Repair
Condition: Postoperative Urinary Retention
Interventions: Drug: Tamsulosin;   Drug: Placebo Oral Capsule

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Study has passed its completion date and status has not been verified in more than two years.