NCT02049840View on ClinicalTrials.gov

The European Study of Altis Single Incision Sling System for Female Stress Urinary Incontinence

NACompletedINTERVENTIONAL
Enrollment

153

Participants

Timeline

Start Date

December 16, 2013

Primary Completion Date

November 4, 2019

Study Completion Date

July 21, 2021

Conditions
Stress Urinary Incontinence
Interventions
DEVICE

Altis Single Incision Sling System

Altis Single Incision Sling (SIS) System is a permanently implantable synthetic sling for the surgical treatment of Stress Urinary Incontinence

Trial Locations (13)

8025

Isala Klinieken Locatie Sophia, Zwolle

13005

Hôpital de la Conception, Marseille

28040

Fundacion Jimenez Diaz, Madrid

30029

Centre Hospitalier Universitaire Carémeau - Gyneacology, Nîmes

Centre Hospitalier Universitaire Carémeau, Nîmes

46520

Hospital de Sagunto, Sagunto

46600

Hospital Universitario La Ribera, Alzira

67091

Nouvel Hôpital Civil, Strasbourg

69677

Hôpital Femme Mère Enfant, Bron

76031

Centre Hospitalier Universitaire de Rouen - Hôpital Charles Nicolle, Rouen

80331

Isarklinikum, München

81679

Chirurgische Klinik München - Bogenhausen GmbH, München

95122

Ospedale Garibaldi-Nesima, Catania

Sponsors

Lead Sponsor

Coloplast A/S
All Listed Sponsors
lead

Coloplast A/S

INDUSTRY

NCT02049840 - The European Study of Altis Single Incision Sling System for Female Stress Urinary Incontinence | Biotech Hunter | Biotech Hunter