symptomatic uterine leiomyomata embolization post procedural pain epidural analgesia patient controlled analgesia
Conditions
Interventions
Uterine artery embolization
group 1: PCA (morphin + ketamin)
group 2: epidural analgesia (bupivacain/naropin)
both groups: PCM, diclofenac, tramadol
Sponsors
Onze Lieve Vrouwe Gasthuis, Amsterdam (OLVG)
Eligibility
Inclusion criteria
Inclusion criteria: 1. Women 2. >18 years 3. Premenopausal 4. Symptomatic uterine leiomyoma confirmed by ultrasonography 5. Scheduled (and suitable) for uterine artery embolisation
Exclusion criteria
Exclusion criteria: 1. Wish for future pregnancy 2. Allergy to contrast material 3. Suspection of uterine malignancy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| - painrelief (NRS) | — |
Secondary
| Measure | Time frame |
|---|---|
| - factors predicting amount of pain: amount of embolization material used reduction of volume of uterine leiomyoma others: - hospital stay - costs - adverse effects of analgesia - patient overall satisfaction - number of readmissions because of pain | — |
Contacts
Public ContactNanda Meents
Outcome results
None listed