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Taking people in EgyptNo phase

Preventing Ovarian Hyperstimulation Syndrome in Women With PCOS During IVF

Compares two IVF drug protocols to prevent ovarian hyperstimulation syndrome in women with PCOS.

Plain-language title generated from the registry record
Registry title: Ovarian Hyperstimulation Syndrome Prevention

Key facts

Where
Giza, EgyptSee the 2 sites

AI summary: who the study is looking for

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for women with PCOS who are coming for ICSI (a fertility treatment). It tests ways to prevent ovarian hyperstimulation syndrome.

Age
19 Years to 42 Years
Sex
Women only
Disease stage
Polycystic ovary syndrome (PCOS)

Main reasons for not taking part

  • Women who do not have PCOS

Read by machine on 12 November 2026.

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 19 and 42 years old?

Source: NCT06739759, who can take part

Where in Egypt

  • AlgazeerahGiza, EgyptContact: Mahmoud Alalfy, masterTaking people
  • Aljazeerah hospitalGiza, EgyptContact: Mahmoud Alalfy, MDTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Trial details

Who runs it
Aljazeera Hospital
Trial code
NCT06739759
Record updated
18 December 2024
Original description
Ovarian hyperstimulation is a very hazardous complication of ICSIRead full original descriptionShow less

Prophylaxis Against Ovarian Hyperstimulation Syndrome in PCOS Women

Ovarian hyperstimulation is a very hazardous complication of ICSI

Inclusion: Women with PCOS coming for ICSI.

Exclusion: Women who donnot have PCOS.

ClinicalTrials.gov NCT06739759