postoperative pain
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: ASA I or II surgical sterilization > 18 years Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range 80 F.1.3 Elderly (>=65 years) no F.1.3.1 Number of subjects for this age range
Exclusion criteria
Exclusion criteria: allergy to lidocaine chronic use op opioids liver and renal insuffiency
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Main Objective: Is the perioperative IV administration of lidocaine an effective treatment to reduce postoperative pain after surgical sterilization.;Secondary Objective: Does the IV administration of lidocaine during the perioperative period reduce: - the incidence of postoperative pain - the consumption of co-analgesics - the incidence of PONV - the length of hospital stay;Primary end point(s): Is the continuous systemic perioperative administration of lidocain effective to treat visceral pain after lararoscopic sterilisation in daycare ?;Timepoint(s) of evaluation of this end point: every 15 min. for the first 2 hours postoperatively | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary end point(s): incidence of PONV less need of analgesics to reduce postoperatvie pain;Timepoint(s) of evaluation of this end point: every 15 min. for the first 2 hours postoperatively | — |
Countries
Belgium
Contacts
University Hospitals Leuven