Anesthesia for day-case arthroscopic knee surgery in adult patients.

Anesthesia for day-case arthroscopic knee surgery in adult patients; A comparison of a ultrasound guided sciatic-femoral nerve block with spinal and general anesthesia, a randomized controlled, blinded trial.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON20922

Enrollment

300

Registered

2010-06-13

Start date

2010-07-01

Completion date

Unknown

Last updated

2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anesthesia, Artroscopic knee surgery, Sciatis-femoral nerve block, general anesthesia, spinal anesthesia

Interventions

The patients will get randomized to receive one of the three anesthetic techniques by computer randomization: 1. Spinal anesthesia

2. A sciatic-femoral nerve block

3. General anesthesia.

Eligibility

Inclusion criteria

Inclusion criteria: 1. ASA physical status I – II; 2. Aged 18 – 75 years; 3. Scheduled to have elective ambulatory arthroscopic knee surgery.

Exclusion criteria

Exclusion criteria: 1. Contraindications to regional anesthesia (e.g., allergy, bleeding disorders, localized infection and neurologic disease); 2. Respiratory or cardiac disease; 3. Morbid obesity (body mass index > 35 kg/m2); 4. Diabetes or peripheral neuropathy; 5. Receiving chronic analgesic therapy.

Design outcomes

Primary

Measure	Time frame
The primary outcome measure is time to home discharge.	—

Secondary

Measure	Time frame
Secondary outcomes are duration of preparation and recovery time of the anesthetic technique, surgical conditions with the used anesthetic technique, duration of the surgical procedure and patients satisfaction.	—

Contacts

Public ContactF.H.J. Loon, van

Michelangelolaan 2

rick.v.loon@cze.nl

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)