Skip to main content
Clinical Trials/NL-OMON49995
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

Vrije Universiteit Medisch Centrum0 sites114 target enrollmentTBD

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.

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

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

Similar Trials