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N/A Completed N=30 Randomized Single-blind Prevention

Aspiration of Limited Number of Follicles to Prevent Severe Ovarian Hyperstimulation Syndrome

Source: ClinicalTrials.gov NCT02635425 ↗
Enrolled (actual)
30
Serious AEs
30.0%
Results posted
Apr 2016
Primary outcomePrimary: Number of Participants of Severe Ovarian Hyperstimulation Syndrome — 2; 11 participants

Summary

The purpose of this study is to evaluate the effect of single ovarian puncture to retrieve 7eggs only in prevention of severe ovarian hyperstimulation syndrome.

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants of Severe Ovarian Hyperstimulation Syndrome
2; 11

Eligibility Criteria

Inclusion Criteria

  • More than 9 days of induction of ovulation.
  • Each ovary contains more than 20 follicles.
  • The majority of follicles are >14mm in diameter.
  • Mild fluid in Douglas pouch.
  • The patient started to complain of considerable lower abdominal pains before the egg collection.

Exclusion Criteria

  • Recurrent ICSI failure or bad obstetric history.
  • Any medical disorder affecting the fluid shift as: diabetes mellitus, autoimmune diseases, hepatic, renal or cardiac conditions.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02635425). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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