ID
Bron
Aandoening
umbilical hernia
postoperative pain
rectus sheath block
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
proportion of patients with a pain intensity of 3 or less, as assessed by the NRS
Onderzoeksopzet
10 minutes after arrival at the PACU
30 minutes postoperatively
3, 6, 12 and 24 hours postoperatively.
Onderzoeksproduct en/of interventie
ultrasound guided bilateral rectus sheath block
local wound infiltration.
Publiek
B.P.C.M. van de Ven
De Run 4600
Veldhoven 5504 DB
The Netherlands
Phone (office): 040-888.50.30
Email: d.vandeven@mmc.nl
Wetenschappelijk
B.P.C.M. van de Ven
De Run 4600
Veldhoven 5504 DB
The Netherlands
Phone (office): 040-888.50.30
Email: d.vandeven@mmc.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
Adult (>18 years old)
ASA-classification between I-III,
elective open primary umbilical hernia repair.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
- primary umbilical hernia repair via scopic
surgical technique.
- emergency umbilical hernia repair
- previous history of umbilical hernia repair.
- simultaneous repair of other hernia defects
- other surgical procedures performed during
the primary umbilical hernia repair.
- Patients with an ASA-classification >III.
- Patients with any contraindications for an
ultrasound guided bilateral rectus sheath
block.
- allergy for LA drugs
- chronic treatment with analgesic drugs
- previous history with the medical
subspecialty of Pain Medicine.
- previous history of a laparotomy or stoma.
- no informed consent (IC)
- impaired mental capacity for self-
determination.
Opzet
Deelname
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Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
| Register | ID |
|---|---|
| NTR-new | NL4056 |
| NTR-old | NTR5940 |
| Ander register | METC // CCMO : 15.122 // NL 54946.015.15 |