NL-OMON23062
Not yet recruiting
Not Applicable
A Pilot-study to determine the (cost)effectiveness of the adhesion barrier 4DryField® PH in prevention of dysmenorrhea, pain and niche-related problems after Caesarean sections
Amsterdam UMC, VUmc0 sites110 target enrollmentTBD
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Amsterdam UMC, VUmc
- Enrollment
- 110
- Status
- Not yet recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patients undergoing their first CS (planned or unplanned)
- •\-Age \= 18 years
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
- •\-Patients with chronic abdominal pain
- •\-Patients who do not speak Dutch or English
Outcomes
Primary Outcomes
Not specified
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