Low-Dose Aspirin in in Vitro Fertilization (IVF) and Intracytoplasmic Sperm Injection (ICSI) Treatments

NCT00683202 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 374

Last updated 2008-05-23

No results posted yet for this study

Summary

In this study we hypothesized that low-dose aspirin therapy (100 mg daily) improves ovarian responsiveness, uterine haemodynamics and clinical pregnancy rates in unselected subjects undergoing IVF/ICSI when the treatment is started concomitantly with controlled ovarian hyperstimulation.

Conditions

  • Pregnancy
  • Miscarriage Less Than 12 Gestational Weeks
  • Extrauterine Pregnancy
  • Preeclampsia
  • Intrauterine Fetal Growth Restriction

Interventions

DRUG

Acetylsalicylic acid

Acetylsalicylic acid 100 mg or placebo daily perorally started on the first day of ovarian gonadotrophin stimulation in in vitro fertilization or in intracytoplasmic sperm injection

DRUG

Placebo

Acetylsalicylic acid 100 mg or placebo daily perorally started on the first day of ovarian gonadotrophin stimulation in in vitro fertilization or in intracytoplasmic sperm injection

Sponsors & Collaborators

  • Bayer

    collaborator INDUSTRY
  • Kuopio University Hospital

    collaborator OTHER
  • Tampere University

    collaborator OTHER
  • University of Oulu

    lead OTHER

Principal Investigators

  • Mervi Haapsamo, MD · University Hospital of Oulu, Finland

  • Juha Rasanen, MD · University Hospital of Oulu, Finland and Oregon Health Sciences University, Oregon USA

  • Hannu Martikainen, MD · University Hospital of Oulu, Finland

  • Juha S Tapanainen, Prof · University Hospital of Oulu, Finland

  • Seppo Heinonen, Prof · University Hospital of Kuopio, Finland

  • Helena Tinkanen, MD · Unversity Hospital of Tampere, Finland

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
39 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2001-03-31
Primary Completion
2006-03-31
Completion
2006-03-31

Countries

  • Finland

Study Locations

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Entities

Drugs
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00683202 on ClinicalTrials.gov