NCT01892826

Brief Summary

The rational of the study is to assess the pregnancy rate after the transfer of frozen blastocyst in natural cycle controlled by external administration of hCG.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
120

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Feb 2009

Longer than P75 for not_applicable

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2009

Completed
3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2012

Completed
1.1 years until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2013

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

July 1, 2013

Completed
3 days until next milestone

First Posted

Study publicly available on registry

July 4, 2013

Completed
Last Updated

July 4, 2013

Status Verified

July 1, 2013

Enrollment Period

3 years

First QC Date

July 1, 2013

Last Update Submit

July 3, 2013

Conditions

Keywords

FETBlastocystnatural cyclehCGSpontaneous LH pic

Outcome Measures

Primary Outcomes (1)

  • Implantation rate

    2 years

Secondary Outcomes (1)

  • ongoing pregnancy rate

    2 years

Study Arms (2)

hCG group

EXPERIMENTAL
Drug: hCG

LH pic

NO INTERVENTION

Interventions

hCGDRUG

5000IU

hCG group

Eligibility Criteria

Age17 Years - 40 Years
Sexfemale
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • age \< 40
  • BMI:18-29 kg/m2
  • day 5 frozen embryo
  • previously IVF/ICSI

You may not qualify if:

  • OOCYTE DONATION CYCLES

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Infertility

Condition Hierarchy (Ancestors)

Genital DiseasesUrogenital Diseases

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Kyrou Dimitra

Study Record Dates

First Submitted

July 1, 2013

First Posted

July 4, 2013

Study Start

February 1, 2009

Primary Completion

February 1, 2012

Study Completion

March 1, 2013

Last Updated

July 4, 2013

Record last verified: 2013-07