Chu Grenoble Alpes
Chu Grenoble Alpes
Grenoble, France4 results ยท Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Urinary and Sexual Symptoms in Patients With Hirschsprung Disease | Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Abnormalities, Digestive System Diseases, Genital Diseases, Hirschsprung disease, Lower Urinary Tract Symptoms, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, Urogenital Diseases, Urological Manifestations, colonic disorder, digestive system disorder, intestinal disorder, megacolon, physiological sexual disorder | Not yet recruiting | Not stated | 2026-08-03 | NCT07742436 | |
| Intermediate Versus Standard Dose Enoxaparin to Prevent Venous Thromboembolism in Severe Trauma Patients: a Multicenter Double Blind Randomised Controlled Trial | Embolism and Thrombosis, Thromboembolism, cardiovascular disorder, injury, vascular disorder, venous thromboembolism | Not yet recruiting | Not applicable | 2026-04-29 | NCT07506473 | |
| Evaluation of the Non-inferiority of Resorbable Gelatin Embolization Compared to Embolization Combined With Endometrial Aspiration for the Management of Hemorrhagic Uterine Vascular Abnormalities Following Premature Termination of Pregnancy | Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Genital Diseases, Hemorrhage, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Urogenital Diseases, Uterine Hemorrhage, Vaginal Bleeding, female reproductive system disorder, uterine anomalies, uterine disorder | Not yet recruiting | Not applicable | 2025-10-03 | NCT07206342 | |
| Adapting the FACETS Program to Sickle Cell Disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Fatigue, Hemic and Lymphatic Diseases, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, anemia, familial hemolytic anemia, hematologic disorder, hemolytic anemia, hereditary disease, inherited hemoglobinopathy, sickle cell disease | Recruiting | Not applicable | 2025-08-19 | NCT06650813 |