Temporally Splitting Ovarian Stimulation and Embryo Transfer

NCT ID: NCT00795041

Last Updated: 2010-10-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

10 participants

Study Classification

OBSERVATIONAL

Study Start Date

2008-11-30

Study Completion Date

2010-09-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The purpose of this study is to explore the concept of temporally splitting ovarian stimulation and embryo transfer.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Splitting of Ovarianstimulation and Embryotransfer

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

1

10 women with indication for ART with ICSI or IVF

No interventions assigned to this group

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Indication for IVF/ICSI
* Age 18-36 years
* \<= three earlier unsuccessful IVF/ICSI treatments with embryo transfer
* BMI 20-30
* Regular cycle with ovulation (28-35 days)
* Progesterone \>7ng/ml at the beginning of stimulation
* Informed consents

Exclusion Criteria

* PCOS (polycystic ovarian syndrome
* Endometrioses \>= grade 3
* Known poor response syndrome
* History of ovariectomy
* Severe endocrinopathie
Minimum Eligible Age

18 Years

Maximum Eligible Age

36 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

University of Luebeck

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

University Hospital of SH, Campus Luebeck, Deparment of Obstetrics/Gynecology

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Georg Griesinger, PD MD

Role: PRINCIPAL_INVESTIGATOR

University of Schleswig-Holstein, Campus Luebeck, Department of Obstetrics and Gynecology

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

University Hospital of Schleswig Holstein, Campus Luebeck, Department of Obstetrics and Gynecology

Lübeck, Schleswig-Holstein, Germany

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Germany

References

Explore related publications, articles, or registry entries linked to this study.

Buendgen NK, Schultze-Mosgau A, Cordes T, Diedrich K, Griesinger G. Initiation of ovarian stimulation independent of the menstrual cycle: a case-control study. Arch Gynecol Obstet. 2013 Oct;288(4):901-4. doi: 10.1007/s00404-013-2794-z. Epub 2013 Apr 3.

Reference Type DERIVED
PMID: 23545834 (View on PubMed)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

TS1

Identifier Type: -

Identifier Source: org_study_id