Ambulatory Lumbar Disk Surgery

Epidural Anesthesia Versus General Anesthesia for Elective Lumbar Disk Surgery in a Outpatient Basis

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT02807194

Enrollment

Registered

2016-06-21

Start date

2014-03-31

Completion date

Unknown

Last updated

2016-06-22

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

Conditions

Lumbar Disk Surgery

Brief summary

Primary Goal: To compare the clinical outcomes of spinal anesthesia and general anesthesia in surgery for lumbar disc herniation.

Detailed description

Patients included: All patients in the neurosurgery department of the University Hospital of Reims or in the neurosurgery department of CHG Chalons en Champagne for surgical management of lumbar disc herniation and agreeing to participate in the research. The types of anesthesia (general anesthesia or spinal anesthesia) will be randomized. Investigation Plan: Participation in the research will be available to any eligible patient during the anesthesia consultation prior hospitalization for surgery. If the patient agrees to participate in research, randomization of the anesthetic technique will be realized. The anesthetist and the patient will be informed of the outcome of this randomization. Hospitalization of patients will not be changed. They will be hospitalized in inpatient, as usual, with an entry the day before surgery and an outlet the next day (without complications). The surgery itself will not be changed. The patient's postoperative monitoring will not be changed. Data will be collected for each patient: demographic data, medical data, data about the intervention and anesthesia, postoperative data management.

Interventions

OTHERspinal anesthesia

OTHERgeneral anesthesia

PROCEDURElumbar disc herniation

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

SUPPORTIVE_CARE

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* single lumbar disk herniation elective for surgery

Exclusion criteria

* Patients with haemostatic disorder * Patients with lumbar spine surgery history * Patients with sciatica called hyperalgesia resistant to treatment including systemic corticosteroids and 3 WHO bearing analgesics (oral morphine) * Patients with true paralyzing sciatica with motor disorders compatible with the path of the root compressed by the herniation * Patients with sphincter disorders * Patients with herniated disc multistage * Pregnant women * Patients with comorbid against-showing the elongated position, including cardiorespiratory comorbidities * Minors patients * Patients protected by law.

Design outcomes

Primary

Measure	Time frame
consumption of analgesic Level III (according to WHO criteria)	24hours

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026