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The Effect of Clindamycin and a Live Biotherapeutic on the Reproductive Outcomes of IVF Patients With Abnormal Vaginal Microbiota

A Double-blind, Placebo-controlled Multicenter Trial on the Effect of Clindamycin and a Live Biotherapeutic on the Reproductive Outcomes of IVF Patients With Abnormal Vaginal Microbiota

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05166746
Enrollment
333
Registered
2021-12-22
Start date
2017-12-07
Completion date
2023-10-01
Last updated
2023-07-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bacterial Vaginoses, Infertility, Female

Brief summary

Study question: Does antibiotic alone or in combination with live biotherapeutic treatment of an abnormal vaginal microbiota improve the reproductive outcomes of IVF couples? Study hypothesis: The investigator hypothesize that treatment of the reproductive tract pathogens and restoration of vaginal Lactobacillus will improve the reproductive outcomes of IVF patients. What is known already? Ultra-deep sequencing methods enable the refinement of reproductive tract microbiology in infertile patients. A recent meta-analysis reported that 19% of infertile patients had abnormal vaginal microbiota Moreover, someone have detected the presence of a Gardnerella (G.) vaginalis dominated endometrial biofilm in 50% of non-infertile patients with abnormal vaginal microbiota undergoing curettage; thus the treatment of such an endometrial biofilm might play an important role for the endometrial receptivity and subsequently the clinical pregnancy rate. Pilot study: In a recent pilot study it was observed that an abnormal vaginal microbiota negatively affects the clinical pregnancy rate in IVF patients. In this study the prevalence of abnormal vaginal microbiota was 28% (36/130) and only 9% of patients with qPCR defined abnormal vaginal microbiota obtained a clinical pregnancy (p=0.004). This association remained significant in an adjusted analysis. Furthermore, the invetigators have preliminary results demonstrating that vaginal bacteria such as G. vaginalis can be found in the endometrium of IVF patients, which is also supported by recent publications What is the novelty of this study? To the investigators knowledge, no previous treatment study of abnormal reproductive tract microbiota has been performed in IVF patients; this relatively small intervention holds the potential to increase the baby-take-home rate after IVF treatment.

Interventions

DRUGClindamycin

Oral clindamycin 300mg/2xdaily in 7 days. LACTIN-V applicators 1x at night in 7 days, then 2xper week at night for 7 weeks.

OTHERPlacebo

The Clindamycin placebo appear identical to active clindamycin by filling capsules with Mannitolium. The LACTIN-V placebo product has no intrinsic effect and is used to study the effect of the therapeutically active product. It is supplied as a pre-filled vaginal applicator packaged under nitrogen gas with one desiccant packet (0.25 g) in a sealed foil pouch. Each applicator contains 200 mg of LACTIN-V placebo powder containing the inactive ingredients of the LACTIN-V drug product, but not Lactobacillus crispatus CTV-05 (CTV-05), the active ingedient. The excipients used in the manufacture of LACTIN-V placebo are identical to those in the LACTIN-V drug product. Each placebo applicator contains the following constituents: maltodextrin, trehalose, xylitol, colloidal silicon dioxide, and sodium ascorbate

Sponsors

Peter Humaidan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Masking description

Moreover, an interim analysis will be performed by blinded outcomes assessors according to the primary outcome.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 42 Years
Healthy volunteers
No

Inclusion criteria

* Abnormal vaginal microbiota. * The screening swab should be repeated if more than 3 months old. * HIV, Hepatitis B or C positivity. * First, second or third IVF stimulation cycle or embryo transfer therefrom. * BMI\<35 * Written informed consent.

Exclusion criteria

* Known or suspected hypersensitivity to clindamycin. * HPV CIN 2 or higher. * Former or current inflammatory bowel disease * Severe concomitant disease, including diabetes. * MAX 2 embryos may be transferred * Artificial heart valve * Intrauterine malformations with operation indication as determined by treating physician (Polyps, Septum, fibroma)

Design outcomes

Primary

MeasureTime frameDescription
Rate of clinical pregnancy per embryo transfer7-9 weeksUltrasound scan detection of intrauterine fetal heartbeat in gestational week 7-9

Secondary

MeasureTime frameDescription
Live birth rate25-42 weeks depending on pregnancy.The birth of a live born child after 25 gestational weeks.
Biochemical pregnancy14 days gestationpositive hCG blood test
Implantation ratepregnancy scan at 7-9 weeksThe number of embryos implanting
Cure of abnormal vaginal microbiota1-2 monthsA vaginal swab and qPCR-validated diagnostics for abnormal vaginal microbiota
Number of late miscarriage12 weeks gestation - to labour (i.e. not including still birth)The of pregnancy in late pregnancy
Number of preterm birthprior to 37 gestational weeksbirth of a liveborn
Birth weight25-42 weeks gestation depending on pregnancyweight at birth
early miscarriage14 days - 12 weeks gestationThe loss of an hCG positive pregnancy

Countries

Denmark

Contacts

Primary ContactThor Haahr, MD
thohaa@rm.dk+4527885402

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026