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CompletedNCT02351193Updated Feb 2, 2015

a Predictive Scheme for Poor Responders in IVF Cycles

An observational study in Infertility, sponsored by Dina Mohamed Refaat Dakhly. Completed at 1 site in Egypt. Open to female participants aged 20 Years to 45 Years. Per ClinicalTrials.gov, last updated 2015-02-02.

Sponsored by Dina Mohamed Refaat Dakhly · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
928
Ages
20 Years to 45 Years
Sex
Female
01

Study summary

While practicing the different assisted reproductive techniques, the investigators are faced daily by the problem of poor responder females, and the debate about predicting its results based on the outcome of the different ORTs used. Due to the cost of AMH as an indicator for ovarian response, the need to re-assess its role was essential in our community, which led us to conduct this prospective multi-center IVF study.

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Conditions studied

  • Infertility

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In context

Infertility

2,506 studies on the registry are indexed under Infertility; 407 are open to participants now.

This study's enrollment of 928 is above the median of 200 across 714 observational studies indexed under Infertility.

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Lead sponsor

This is the only study on the registry with Dina Mohamed Refaat Dakhly as lead sponsor.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
20 Years to 45 Years
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Poor responder females

Inclusion criteria

  • normal body mass index (BMI)
  • AMH from 0.5-1.1 ng/ml.
  • previous history of ≤3 oocytes retrieved using conventional long stimulation protocol

Exclusion criteria

Exclusion Criteria:

  • Females suffering from other causes of infertility as tubal, uterine factors or known cases of endometriosis
  • severe cases of male factor as azospermia
  • females who were unable or not willing to participate in the study were excluded from the study.
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
928 participants (actual)
Patient registry
No

Groups and cohorts

  • Group I

    poor responder females with age less than 35

    Other: transvaginal Ultrasound

  • Group II

    poor responder females with age more than 35

    Other: transvaginal Ultrasound

Interventions

  • Othertransvaginal Ultrasound
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What researchers measure

Primary outcomes

  1. Number of MII oocytes

    Time frame: 2 years

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Study locations

1 site
  • Kasr el aini hospital
    Cairo, Egypt
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 2, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02351193
Lead sponsor
Dina Mohamed Refaat Dakhly
Responsible party
Dina Mohamed Refaat Dakhly (Lecturer of Obstetrics and Gynecology, Woman's Health University Hospital, Egypt) — Sponsor-investigator
First posted
Jan 30, 2015
Start date
Jan 2011
Primary completion
Dec 2013
Completion
Dec 2013
Last update
Feb 2, 2015

Study contacts

Dina MR Dakhly, MD
principal investigator · Cairo University

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2015. You cannot join it, but the record below documents what was studied.

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