Mental wellbeing and quality of life after insertion of a LNG-IUD or Cu-IUD. A randomized patient preference trial.

Recruiting

• Conditions: anticonceptie; well-being; quality of life; 10018515

• Registration Number: NL-OMON48848
• Lead Sponsor: oordwest Ziekenhuisgroep

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 15 April 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: 394

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

Study & Design

• Study Type: Interventional
• Study Design: Not specified