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UnknownNCT03080740

The Efficacy and Safety Study of Clindamycin Palmitate Hydrochloride Dispersible Tablet Treatment of Bacterial Vaginosis

The Efficacy and Safety Study of Clindamycin Palmitate Hydrochloride Dispersible Tablet for the Treatment of Bacterial Vaginosis

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
300 (estimated)
Sponsor
Guangzhou Yipinhong Pharmaceutical CO.,LTD · Industry
Sex
Female
Age
18 Years – 55 Years
Healthy volunteers
Not accepted

Summary

Randomized, double blind, positive drug parallel comparison, multi-centre clinical trial to assess the Efficacy and Safety of Clindamycin palmitate hydrochloride dispersible tablet for the treatment of bacterial vaginosis

Detailed description

Treatment group: Clindamycin palmitate hydrochloride dispersible tablet . Control group: Metronidazole Tablet.

Conditions

Interventions

TypeNameDescription
DRUGClindamycin palmitate hydrochloride dispersible tablet300mg, oral after meal, twice daily, a total of 7days
DRUGMetronidazole Tablet400mg, oral after meal , twice daily, a total of 7days

Timeline

Start date
2016-07-01
Primary completion
2017-07-01
Completion
2017-12-01
First posted
2017-03-15
Last updated
2017-03-15

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT03080740. Inclusion in this directory is not an endorsement.

The Efficacy and Safety Study of Clindamycin Palmitate Hydrochloride Dispersible Tablet Treatment of Bacterial Vaginosis (NCT03080740) · Clinical Trials Directory