NL-OMON49995
Recruiting
Not Applicable
A Pilot-study to determine the (cost) effectiveness of the adhesion barrier 4DryField® PH in prevention of dysmenorrhea, abdominaal pain and niche-related problems after caesarean sections - 4DryField Study
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Adhesions
- Sponsor
- Vrije Universiteit Medisch Centrum
- Enrollment
- 114
- Status
- Recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •\- Patients who underwent their first CS (primary or secondary)
- •\- Sufficient command of the Dutch or English language
- •\- \>\= 18 years old
Exclusion Criteria
- •\- Patients with an indication for an emergency CS (suspicion of fetal
- •distress), or patients in heavy pain without accurate therapy, and who were not
- •informed about this study during pregnancy
- •\- Previous uterine major surgery (e.g. laparoscopic or fibroid resection by
- •laparotomy, septum resection)
- •\- Patients with known causes of menstrual disorders (known cervical dysplasia,
- •communicating hydrosalpinx, uterine anomaly or endocrine disorders disturbing
- •ovulation) or use of medication that can influence the frequency of blood loss
- •(e.g. Ascal).
- •\- Placenta percreta during the current pregnancy
Outcomes
Primary Outcomes
Not specified
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