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Montelukast for Prevention & Treatment of OHSS

Montelukast for Prevention & Treatment of Ovarian Hyperstimulation Syndrome in Freeze-all Cycles

Status
Suspended
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03794037
Enrollment
20
Registered
2019-01-04
Start date
2018-12-05
Completion date
2023-12-31
Last updated
2022-09-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ovarian Hyperstimulation Syndrome

Keywords

ovarian hyperstimulation syndrome, Montelukast

Brief summary

montelukast & dydrgesteron will be given to cases with suspected or proven ovarian hyperstimulation in one group in comparison with dydrogesteron alone in the other group.

Detailed description

patients with high risk for ovarian hyperstimulation will undergo a freeze-all protocol then montelukast & dydrgesteron will be given to cases with suspected or proven ovarian hyperstimulation in one group in comparison with dydrogesteron alone in the other group.

Interventions

DRUGdydrgesterone 10 mg( tab)/12hs/14 days

Dydrogesterone Oral Tablet 10 mg twice daily for 14 days to be taken from the day of ovum pickup

COMBINATION_PRODUCTmontelukast 10 mg(tab) oral/24hs/ 7 days dydrgesterone 10 mg( tab) oral/12hs/14 days

montelukast 10 mg(tab) once daily oral for 7 days & dydrgesterone 10 mg (tab) twice daily oral for 14 days &

Sponsors

Hawaa Fertility Center
CollaboratorOTHER
Benha University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 37 Years
Healthy volunteers
No

Inclusion criteria

* PCOS high responders high numbers of ovum retrieved

Exclusion criteria

* hypersensitivity to any drug components phenylketonuria patients depression liver dysfunction

Design outcomes

Primary

MeasureTime frameDescription
Number of Participants who develop ovarian hyperstimulation syndrome0-14 daysincidence

Secondary

MeasureTime frameDescription
Number of Participants treated of ovarian hyperstimulation syndrome0-14 daystreatment & resolution

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026