Abnormal Vaginal Flora Clinical Trial
Official title:
Comparison Between Oral Clindamycin Vs Metronidazole for the Treatment of Abnormal Vaginal Flora in High Risk Pregnancies
Verified date | June 2024 |
Source | HaEmek Medical Center, Israel |
Contact | Zohar Nachum, MD |
Phone | 972-46495483 |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Abnormal vaginal flora is a risk factor for preterm labor. Therefore, in high risk pregnancies for preterm labor the diagnosis and treatment of abnormal flora is indicated. Clindamycin and metronidazole given orally are both acceptable treatments in these cases. The purpose of this study is to compare the effectiveness of Clindamycin Vs metronidazole for the treatment of abnormal vaginal flora in high risk pregnancies. For this purpose, pregnant women who are considered high risk for preterm labor and were diagnosed with abnormal vaginal flora will be randomly treated either with clindamycin or metronidazole. Eradication of the abnormal flora and adverse effects will be monitored and compared
Status | Recruiting |
Enrollment | 750 |
Est. completion date | August 1, 2025 |
Est. primary completion date | August 1, 2025 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 50 Years |
Eligibility | Inclusion Criteria: - Pregnant women at increased risk for preterm labor (preterm cervical effacement, preterm uterine contractions, twins pregnancy, vaginal bleeding, past preterm delivery) - Age above 18 years Exclusion Criteria: - Known allergy to the tested antibiotics - Antibacterial treatment in the week before the vaginal culture was taken - preterm premature rupture of membranes |
Country | Name | City | State |
---|---|---|---|
Israel | Departement of obstetric and gynecology, HaEmek medical center | Afula | |
Israel | Departement of obstetric and gynecology, Poriya Medical Center | Tiberias |
Lead Sponsor | Collaborator |
---|---|
HaEmek Medical Center, Israel |
Israel,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | To compare the efficacy between oral Clindamycin Vs Metronidazole in the eradication of abnormal vaginal flora | Primary outcome will be assessed by taking a vaginal culture sample a week after one-week antibacterial treatment | ||
Secondary | The prevalence of adverse effects | During the antibacterial treatment which is 1 week of therapy | ||
Secondary | The prevalence of late abortions and preterm deliveries | From date of randomization until the date of delivery or abortion, assessed up to 28 weeks | ||
Secondary | Assessing the correlation between Nugent score , physical examination and Ph indicators | The outcome is assessed after the diagnosis of abnormal vaginal flora is made at 14-26 weeks of gestation |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT01287728 -
The Value of Bacterial Loads by Real Time PCR in Predicting Recurrence of Abnormal Vaginal Flora After Oral Metronidazole Therapy
|
Phase 3 |