Effect of low-dose aspirin on OHSS

Effect of low-dose aspirin before IVF to prevent ovarian hyperstimulation syndrome (OHSS)

Status

Recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT20210730052019N2

Enrollment

Registered

2021-08-28

Start date

2021-08-25

Completion date

Unknown

Last updated

2021-08-30

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

Conditions

Infertility. Female infertility

Interventions

Intervention group: The study will be conducted in Kerman Afzalipoor Hospital. The intervention group will be administered low dose ASA two weeks before the start of menstural cycle and will recieve C

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Female patients planned to treat with anatgonist protocol ART (Assisted Reproductive Technology) Having PCO criteria (Including AMH level more than 4 ng/ml, Sonogram suggestive of PCO, and Oligomenorrhea)

Exclusion criteria

Exclusion criteria: Lack of consent to participate

Design outcomes

Primary

Measure	Time frame
OHSS Incidence. Timepoint: Throughout the study based on patients symptoms or on the third day after punction based on laboratory and sonographic findings. Method of measurement: Patient symptoms montioring sheets - Laboratory findings (Rise of liver enzymes, creatinine, hematocrit), sonographic findings (ascites).;OHSS Severity. Timepoint: Throughout the study based on patients symptoms or on the third day after punction based on laboratory and sonographic findings. Method of measurement: Patient symptoms montioring sheets - Laboratory findings (Rise of liver enzymes, creatinine, hematocrit), sonographic findings (ascites).	—

Measure

Time frame

OHSS Incidence. Timepoint: Throughout the study based on patients symptoms or on the third day after punction based on laboratory and sonographic findings. Method of measurement: Patient symptoms montioring sheets - Laboratory findings (Rise of liver enzymes, creatinine, hematocrit), sonographic findings (ascites).;OHSS Severity. Timepoint: Throughout the study based on patients symptoms or on the third day after punction based on laboratory and sonographic findings. Method of measurement: Patient symptoms montioring sheets - Laboratory findings (Rise of liver enzymes, creatinine, hematocrit), sonographic findings (ascites).

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactVictoria Habibzadeh

Kerman University of Medical Sciences

v_habibzadeh@kmu.ac.ir+98 34 3132 8000

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026