Viewing Study NCT06411314



Ignite Creation Date: 2024-05-19 @ 5:33 PM
Last Modification Date: 2024-10-26 @ 3:29 PM
Study NCT ID: NCT06411314
Status: COMPLETED
Last Update Posted: 2024-05-13
First Post: 2024-05-08

Brief Title: Efficacy and Safety of Natamycin and Lactulose Vaginal Suppositories in Treatment of Vulvovaginal Candidiasis
Sponsor: Avva Rus JSC
Organization: Avva Rus JSC

Study Overview

Official Title: Efficacy and Safety of Vaginal Suppositories Containing Combination of Natamycin and Lactulose in Treatment of Vulvovaginal Candidiasis International Randomized Controlled Superiority Clinical Trial
Status: COMPLETED
Status Verified Date: 2024-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose is to study superior efficacy of combination of Natamycin and Lactulose Natamycin 100 mg Lactulose 300 mg vaginal suppositories compared to Pimafucin Natamycin 100 mg vaginal suppositories or Lactulose 300 mg vaginal suppositories The second objective of the study was to investigate the safety of the combination suppositories in the treatment of vulvovaginal candidiasis in non-pregnant adult females
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None