Postanesthetic transitory neurologic syndrome
Conditions
Interventions
Trade Name: MAGNESIO LAVOISIER
Pharmaceutical Form: Solution for injection/infusion
Trade Name: Fentanest
Pharmaceutical Form: Solution for injection/infusion
Sponsors
Hospital General de Ciudad Real
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Same day surgery 2. Both genders. Pregnancy in fertile women ruled out by serum or urine check preoperatively. 3. Operated in lithotomy position or 4. Arthroscopy position or 5. Obese in any position, with infraumbilical incision 6. Spinal lidocaine anesthetic aine anesthesia 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 60 F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range 20
Exclusion criteria
Exclusion criteria: a) Younger than 18 years old or older than 80 years old. b) American Society of Anesthesia class 3 or 4 c) Active low back pain d) Any myopathy or neuropathy e) Pregnant or breast-feeding women f) Known allergy or sensitivity to lidocaine, magnesium or fentanyl g) Known intracardiac electrical conduction defect seen in the electrocardiogram
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Main Objective: Determine rate of postanesthetic transitory neurologic syndrome (buttocks pain);Secondary Objective: 1. Time to home discharge 2. Duration of sensitive block 3. Ammount of postoperative analgesia needed 4. Duration of motor block 5. Time to voiding 6. Time to oral intake 7. Posoperative nausea(vomiting rate 8. Inadequate anesthesia rate and conversion to general anesyhesia 9. Rate of unexpected ward admisssion and reason for;Primary end point(s): Postoperative Transitory neurologic syndrome (buttocks pain) rate;Timepoint(s) of evaluation of this end point: Second, fourth and sixth posoperative day | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary end point(s): 1. Time to home discharge 2. Duration of sensitive block 3. Ammount of postoperative analgesia needed 4. Duration of motor block 5. Time to voiding 6. Time to oral intake 7.Posoperative nausea/vomiting rate 8. Inadequate anesthesia rate and conversion to general anesyhesia 9. Rate of unexpected ward admisssio and reason;Timepoint(s) of evaluation of this end point: Inmediate postoperative hours till dischage from the unit | — |
Countries
Spain
Contacts
Public ContactUnidad de Investigación
Hospital General Universitario de Ciudad Real
Outcome results
None listed