CClinicalTrials.gg
Status unknownNCT04539067Updated Sep 4, 2020

Effect of Controlled Ovarian Stimulation in Quality of Oocyte and Embryo

A Phase 2 interventional study of HHMG in Ovarian Stimulation, sponsored by Minia University. Status unknown. Open to female participants aged 20 Years to 35 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2020-09-04.

Sponsored by Minia University · Phase 2, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Aug 2020), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Phase 2
Study type
Interventional
Enrollment
70
Allocation
Randomized
Ages
20 Years to 35 Years
Sex
Female
01

Study summary

Investigate and compare the efficacy of H FSH plus HMG Vs HMG alone on oocyte and embryo quality in IcsI patients

Read the detailed description

70 patients divided in to 2groups Group A controlled ovarian stimulation with H FSH and HHMg Group B controlled ovarian stimulation with HMG alone Results will be discussed later

02

Conditions studied

  • Ovarian Stimulation
03

In context

Lead sponsor

Minia University is the lead sponsor of 356 studies on the registry; 115 are open to participants now.

Of its 6 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

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

04

Who can participate

Ages eligible
20 Years to 35 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Inclusion criteria

  1. Infertil women aged from 20_35yr
  2. Normal utreus
  3. Normal ovaries
  4. unexplained infertility
  5. no endometriosis

Exclusion criteria

Exclusion Criteria:

1 - poor responders to gonadotropin 2-Prior history of more than 3unsucceful ICSI 3-Any malformation of sexual organs

05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
70 participants (estimated)

Study arms

  • Experimental
    HMG group

    Induction of ovulation from 2nd day of cycle Follow diameter of follicle When follicle 18:22mm Receive HMG

    Drug: HHMG

  • Experimental
    H FSH plus HHMG

    Follow up ovulation from the 2nd day to 5th of menstruation cycle When follicle diameter 18mm to 22mm made induction of ovulation

    Drug: HHMG

Interventions

  • DrugHHMG

    Induction of ovulation from the 2nd day of cycle to 5th day then follow the diameter of follicle Use transvaginal ultrasound When diameter of follicle 18 to 22 patients receiving HMG

    Also known as: Using HHMG for induction

06

What researchers measure

Primary outcomes

  1. Comparison between the efficacy of controlled ovarian stimulation with H FSH plus HMG Vs HmG alone on oocyte and embryo quality in IcsI patients

    Comparison between the efficacy of controlled ovarian stimulation with H FSH plus HMG Vs HmG alone on oocyte and embryo quality in IcsI patients

    Time frame: 9 months

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 4, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT04539067
Lead sponsor
Minia University
Responsible party
Marwa Bahgat Tarahony (Eygpt Minia, Minia University) — Principal investigator
First posted
Sep 4, 2020
Start date
Sep 1, 2020 (estimated)
Primary completion
Sep 2021 (estimated)
Completion
Oct 2021 (estimated)
Last update
Sep 4, 2020

Study contacts

Marwa Ba Tarahony
Contact
marwatarahony9@gmail.com
01008160037
Kareem Ib Shaheen
Contact
01210966045
Marwa Ba Tarahony
principal investigator · Faculty of Medicine, Minia University

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Aug 2020. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion