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Clinical Trials/NL-OMON23062
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.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
Amsterdam UMC, VUmc

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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