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Ovarian Hyperstimulation Syndrome Prevention (OHSS)

A

Aljazeera Hospital

Status

Enrolling

Conditions

Ovarian Hyper Stimulation Syndrome (OHSS)

Treatments

Drug: Modified Agonist protocol for IVF with additive treatments as HCQ
Drug: Antagonist protocol for IVF

Study type

Interventional

Funder types

Other

Identifiers

NCT06739759
ovarian hyperstimulation

Details and patient eligibility

About

Ovarian hyperstimulation is a very hazardous complication of ICSI

Full description

Ovarian hyperstimulation could be mild , moderate , severe or marked

Enrollment

300 estimated patients

Sex

Female

Ages

19 to 42 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Women with PCOS coming for ICSI

Exclusion criteria

  • Women who donnot have PCOS

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

300 participants in 2 patient groups

antagonist
Active Comparator group
Description:
patients with PCOS undergoing ICSI receiving antagonist protocol
Treatment:
Drug: Antagonist protocol for IVF
Modified agonist with additives
Active Comparator group
Description:
Patients with PCOS undergoing ICSI receiving modified agonist protocol with additives
Treatment:
Drug: Modified Agonist protocol for IVF with additive treatments as HCQ

Trial contacts and locations

2

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Central trial contact

Ahmed Elgazzar, MD; Mahmoud Alalfy, MD

Data sourced from clinicaltrials.gov

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