Endometriosis, SHiP, hemoperitoneum, pregnancy
Conditions
Interventions
Questionnaires (SF-36, SVL, UCL, PRISM-RII) and an individual face-to-face in-depth interview will be carried out.
Sponsors
VU University Medical Center Amsterdam
Eligibility
Inclusion criteria
Inclusion criteria: Eleven women with SHiP in their obstetrical history, who already gave written permission to include their case in our previous case-series, will be asked to participate in this trial. Partners will be asked separately if they are willing to participate.
Exclusion criteria
Exclusion criteria: If women or their partners are unable or unwilling to give informed consent, they will be excluded from participation in this trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The aim of this study is to gain better insight in the psychological and functional recovery of women, and their partners, after SHIP. | — |
Secondary
| Measure | Time frame |
|---|---|
| This study will further assess personality characteristics, illness perception, coping strategies and QOL of women, and their partners, after SHIP. | — |
Contacts
Public ContactMarit Lier
VU Medical Centre Boelelaan 1118
Outcome results
None listed