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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04067531
Other study ID # 12
Secondary ID
Status Recruiting
Phase Phase 3
First received
Last updated
Start date August 1, 2020
Est. completion date December 1, 2021

Study information

Verified date March 2020
Source Skaraborg Hospital
Contact P-G Larsson
Phone +46500431000
Email p-g.larsson@vgregion.se
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Treatment of BV with first deqularum cloride and then followed with clindamycin vaginal Cream.


Description:

The hypoteses is that deqularum cloride takes away the biofilm so that clindamycin will kills the bacteria. Cure rate will be followed up after 1 month and then after 6 month


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date December 1, 2021
Est. primary completion date August 1, 2021
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: - healthy women with BV Exclusion Criteria: - women treated with antibiotics within 1 month

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
treatment of BV with first Deqularum and then direkt after with vaginal clindamycin
All patients will get the same treatment

Locations

Country Name City State
Sweden Department of Ob/Gyn, Skaraborgshospital Skövde Skövde

Sponsors (1)

Lead Sponsor Collaborator
Skaraborg Hospital

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary cure of BV cure rate of BV 6 month
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