NCT01933009

Brief Summary

GnRH administration during the luteal phase was found to significantly increase pregnancy rates in women undergoing fresh-cycle IVF cycles. We aim to investigate the effect of GnRH administration during the luteal phase in women undergoing frozen-thawed IVF cycles.

Trial Health

43
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Aug 2013

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

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

August 1, 2013

Completed
27 days until next milestone

First Submitted

Initial submission to the registry

August 28, 2013

Completed
2 days until next milestone

First Posted

Study publicly available on registry

August 30, 2013

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2014

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2014

Completed
Last Updated

August 30, 2013

Status Verified

August 1, 2013

Enrollment Period

9 months

First QC Date

August 28, 2013

Last Update Submit

August 28, 2013

Conditions

Pregnancy Rate

Outcome Measures

Primary Outcomes (1)

  • Pregnancy rate

    1 year

Eligibility Criteria

Age18 Years - 40 Years
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodProbability Sample
Study Population

Women undergoing frozen-thawed IVF cycles

You may qualify if:

  • Frozen-thawed IVF cycles

You may not qualify if:

  • Hydrosalpings Uterine myomas

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

IVF and infertility unit, Assaf Harofeh Medical Center

Ẕerifin, Be'er-Ya'akov, 70300, Israel

RECRUITING

Central Study Contacts

Ido Ben-Ami, MD PhD

CONTACT

972-8-9779005

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
1 Year
Sponsor Type
OTHER GOV
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Dr. Ido Ben-Ami, MD PhD

Study Record Dates

First Submitted

August 28, 2013

First Posted

August 30, 2013

Study Start

August 1, 2013

Primary Completion

May 1, 2014

Study Completion

August 1, 2014

Last Updated

August 30, 2013

Record last verified: 2013-08

Locations

IL(1)