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Atosiban Improves Implantation and Pregnancy Rates in Patients With Repeated Implantation Failure

Atosiban Improves Implantation and Pregnancy Rates in Patients With Repeated Implantation Failure

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01493440
Enrollment
71
Registered
2011-12-16
Start date
2011-03-31
Completion date
2011-09-30
Last updated
2011-12-20

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

Conditions

Repeated Implantation Failure

Keywords

atosiban, clinical pregnancy, implantation rate, uterine contractility, IVF-ET

Brief summary

Atosiban, administered at embryo transfer, can improve the implantation rate and the clinical pregnancy rate in patients with repeated implantation failure undergoing IVF-ET (in-vitro fertilization and embryo transfer).

Detailed description

Atosiban is a mixed oxytocin and vasopressin V1A receptor antagonist.Combined antagonism at oxytocin and vasopressin V1A receptors reduces uterine contractions with a corresponding decrease in intrauterine production of prostaglandin F2alpha and improved uterine blood supply. These effects are of potential benefit for implantation support during IVF-ET cycles.

Interventions

DRUGatosiban

Atosiban was administered as a 6.75mg IV bolus dose 30 minutes prior to embryo transfer followed by a 1-hour IV infusion at dose of 18 mg/h then a 2-hour IV infusion at 6 mg/h.

Sponsors

Vietnam National University
CollaboratorOTHER
An Sinh Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
No

Inclusion criteria

* had repeated implantation failure * have at least 1 good quality embryo for transfer

Exclusion criteria

* uterine abnormalities that could compromise the implantation process (e.g. fibroids, endometrial polyp, bicornuate uterus, adhesion of uterine cavity)

Design outcomes

Primary

MeasureTime frame
Clinical pregnancy5 weeks after intervention

Countries

Vietnam

Outcome results

None listed

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