WHO ICTRP trial
Single-site, open, randomized clinical trial to assess the non-inferiority of…
EUCTR2018-001448-78-ES · EU Clinical Trials Register · Not Recruiting
Key facts
| Trial ID | EUCTR2018-001448-78-ES |
|---|---|
| Public title | Single-site, open, randomized clinical trial to assess the non-inferiority of Cysticlean® versus Fosfomicina in the treatment of cystitis in women in Spain. |
| Scientific title | Single-site, open, randomized clinical trial to assess the non-inferiority of Cysticlean® versus Fosfomicina in the treatment of cystitis in women in Spain. |
| Primary sponsor | Vita Green Europa S.A. |
| Registry | EU Clinical Trials Register |
| Recruitment status | Not Recruiting |
| Study type | Interventional clinical trial of medicinal product |
| Phase | Human pharmacology (Phase I): no Therapeutic exploratory (Phase II): no Therapeutic confirmatory - (Phase III): no Therapeutic use (Phase IV): yes |
| Countries | Spain |
| Conditions | Urinary Tract Infection (UTI) MedDRA version: 20.1 Level: PT Classification code 10011790 Term: Cystitis escherichia System Organ Class: 10021881 - Infections and infestations ;Therapeutic area: Diseases [C] - Female diseases of the urinary… |
| Interventions | Trade Name: Cysticlean Product Name: Cysticlean Product Code: Cyst Pharmaceutical Form: Capsule INN or Proposed INN: cranberry extract Current Sponsor code: Cyst2018_01 Other descriptive name: CRANBERRY Concentration unit: mg milligram(s)… |
| Registration date | Oct 25, 2018 |
| Target size | 128 |
| Secondary IDs | Cyst2018_01 |
| Registry page | clinicaltrialsregister.eu |
At a glance
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About WHO ICTRP trial registrations
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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: