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Clinical Trials/NL-OMON48848
NL-OMON48848
Recruiting
Not Applicable

Mental wellbeing and quality of life after insertion of a LNG-IUD or Cu-IUD. A randomized patient preference trial. - Quality of life after LNG-IUD versus Cu-IUD (E-CHIQ study).

oordwest Ziekenhuisgroep0 sites394 target enrollmentTBD
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Conditionsanticonceptiewell-beingquality of life10018515

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
anticonceptie
Sponsor
oordwest Ziekenhuisgroep
Enrollment
394
Status
Recruiting
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

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
oordwest Ziekenhuisgroep

Eligibility Criteria

Inclusion Criteria

  • •\- Age; between 18 and 45 years.
  • •\- Wish for LARC by means of a LNG\-IUD or Cu\-IUD for a minimum period of 12 months.
  • •\- Willing to fill out 5 questionnaires, taking 15 to 20 minutes per questionnaire.
  • •\- Access to internet and sufficient understanding of Dutch language.
  • •\- Willing to provide informed consent.

Exclusion Criteria

  • •Cu\-IUD insertion as emergency contraception.
  • •Patients with heavy bleeding pattern/problems or with a wish for less blood\-loss.
  • •Patients with an Cu\-IUD or LNG\-IUD \< 3 months prior to placement this IUD
  • •IUD insertion while being under general anaesthetics.
  • •IUD insertion within 6 weeks postpartum and 12 weeks after a caesarean are excluded.
  • •Contraindications according to the product leaflets.
  • •patients taking medication against a mental conditions

Outcomes

Primary Outcomes

Not specified

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