Patient-controlled Sedation During Repair of Obstetric Perineal Lacerations
Pain, Patient Satisfaction
About this trial
This is an interventional supportive care trial for Pain focused on measuring obstetric perineal lacerations, patient-controlled sedation, propofol
Eligibility Criteria
Inclusion Criteria: Adult patient (≥18 years) Planned examination and repair of perineal laceration The patient has after receiving verbal and written information about the study given her signed informed consent to participate Exclusion Criteria: Perineal laceration grade III-IV BMI > 35 (during first visit at the maternity care centre) Deviation from department guidlines regarding preopartive fasting Preeclampsia or hypertensive disease Postpartum haemorrhage > 1000 ml Known/suspected allergy or contraindication to any medication within the study Functional disability in both hands which affect the possibility to operate the PCS device Cognitive impairment, unwillingness or language difficulties resulting in difficulty to understand the meaning of participation in the study or to operate the PCS device
Sites / Locations
- VrinnevihospitalRecruiting
Arms of the Study
Arm 1
Arm 2
No Intervention
Experimental
Control
Patient-controlled sedation with propofol
Clinical routine
PCS group