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Good Responders According to Guidelines Who Wre Charectarized by AMH>0.8ng/dlICSINCT06719817

Evaluation of Some Trace Elements in Follicular Fluid in ICSI Cases and Their Effect on ICSI Outcomes

An observational study of Good Responders According to Guidelines Who Wre Charectarized by AMH>0.8ng/dl and Trace Elements in ICSI Cases, run by Assiut University at 2 sites in Egypt.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

To evaluate concentrations of some trace elements in the follicular fluid and their reproductive outcomes. Read more about this study

Who is it for?
Ages 25 to 40 years, women only
How many people
154 participants
Where
2 sitesEgypt
Study dates
24 Nov 2024to 20 Sep 2026
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 25 to 40 years
  • Women only
  • No healthy volunteers
  • Adult

Study population: good responders according to NICE guidelines with AMH more than 0.8ng/dl and antral follicular count more than 4

Inclusion Criteria:good responders according to NICE guidelines with AMH more than 0.8ng/dl and antral follicular count more than 4 Exclusion Criteria:Poor responders according to ESHRE guidelines as advanced maternal age poor ovarian response and according to NICE guidelines AMH less than 0.8ng/dl

Trial locations and contacts

2 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Fatma Ahmed Waley contact

01064402617

www.fatma.waley@gmail.com

Ahmed Mohammed Nasr contact

01012588888

anasr@edu.eg

Egypt2 sites, 2 recruiting
  • Faculty of medicine

    Asyut, Egypt

    Ahmed Nabil Hassan, 01224532883

    Recruiting
  • Faculty of medicine

    Asyut, Egypt

    Ahmed Mohammed Nasr, Prof, 01012588888

    Recruiting

Other trials in Egypt

About this study

Official title: Evaluation of Some Trace Elements in Follicular Fluid in Intracytoplasmic Sperm Injection(ICSI) Patients

To evaluate concentrations of some trace elements in the follicular fluid and their reproductive outcomes.

Read the detailed description

To evaluate some trace elements in the follicular fluid and their reproductive outcome

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. oocyte maturity

    Millimetres

    Measured: 2024 to 2026

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Dec 2024
  2. Study start24 Nov 2024
  3. Primary completion20 Aug 2026 (estimated)
  4. Study completion20 Sep 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
154 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06719817
Sponsor's protocol ID
AssiutU WHH
Acronym
ICSI
Status last verified
Dec 2024
First submitted
18 Oct 2024
Last updated
6 Dec 2024
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Good Responders According to Guidelines Who Wre Charectarized by AMH>0.8ng/dl and Trace Elements in ICSI Cases, run by Assiut University at 2 sites in Egypt.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 6 Dec 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Fatma Ahmed Waley (01064402617, www.fatma.waley@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

oocyte maturity (time frame: 2024 to 2026). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Dec 2024.

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