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Use of IMSI in Poor Responders to IVF

NCT02358733 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2019-02-28

No results posted yet for this study

Summary

This is a pilot study which aims to determine the role of IMSI in poor responders.

Conditions

  • Female Infertility

Interventions

PROCEDURE

Intra-cytoplasmic Sperm Injection

Selection of sperm at 400x for sperm injection

PROCEDURE

Intra-cytoplasmic Morphologically-selected Sperm Injection

Selection of sperm at 6000x for sperm injection

Sponsors & Collaborators

  • Centro de Infertilidad y Reproducción Humana

    lead OTHER

Principal Investigators

  • Karinna Lattes, MD · Centro de Infertilidad y Reproducción Humana (CIRH)

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
37 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-02-28
Primary Completion
2018-01-31
Completion
2019-02-27

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02358733 on ClinicalTrials.gov