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A Comparative Study Between Lumbar Epidural Analgesia Versus Local Infiltration Anesthesia Combined With Dexmedetomidine Intravenous Infusion in Endoscopic Lumbar Discectomy Surgeries: A Retrospective Study

A

Ain Shams University

Status

Completed

Conditions

Epidural Analgesics for Comparison

Study type

Observational

Funder types

Other

Identifiers

NCT07088016
6/02-2025

Details and patient eligibility

About

The goal of this observational study is to compare the effectiveness and patient satisfaction of local anesthesia combined with intravenous Dexmedetomidine versus epidural anesthesia in endoscopic lumbar discectomy surgeries

Full description

In recent years, with the development of medical instruments, minimally invasive surgical methods for lumbar disc herniation became increasingly popular, such as percutaneous transforaminal endoscopic discectomy (PTED) PTED under local anesthesia (LA) is recommended in consideration of safety. Under LA, patients keep conscious during the procedure, and the surgeon can obtain feedback directly from the patients if the nerve is interfered. However, in clinical practice, we found that many patients couldn't tolerate the pain during operation especially when placing the working channel Dexmedetomidine, a highly selective alpha 2 adrenoreceptor agonist, has unique characteristics in providing sedation and analgesia. Due to its central sympatholytic action, DEX produces dose-dependent sedation, antinociception and anxiolysis, while decreasing intraoperative hypertension and tachycardia episodes Epidural anesthesia is another major method which can keep patients awake during surgery and the surgeons can check the function of the nerve from the maintained motor function of patients' lower limbs

Enrollment

100 patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patients American Society of anesthesiologists' physical status (ASA) I to II.
  2. Aged 18 to 60 years.
  3. Both sexes.
  4. Patients with clinical and radiological evidence of soft disc herniation in a single lumber segment.

Exclusion criteria

  1. Spinal malformation
  2. Recurrent lumber disc herniation (LDH)
  3. Multi segment LDH
  4. Patients younger than 18 years or older than 60 years
  5. Patients with hypersensitivity to one of the used drugs
  6. Patients suffering of coagulopathy
  7. Operation time more than 1 hour

Trial design

100 participants in 2 patient groups

dexmedetomidine group
Description:
loading of Dexmedetomidine was done at a dose of 1 mcg/ kg over 10 minutes followed by continuous infusion at a rate of 0.5 mcg/kg/hr , followed by infiltration of the skin with 2-3 ml of lidocaine hydrochloride 1 % first by the surgeon then an 18 -G needle will be introduced to anesthetize the trajectory with 8-10 ml lidocaine 1 %. After reaching the superior articular process, 2-3 ml of lidocaine 1 % was used to anesthetize the facet joint.
Epidural group
Description:
The epidural insertion point was 2 segments upper than the surgical procedure, 10 ml of Bupivacaine 0.25% was injected in the epidural space to adjust the sensory level. The epidural catheter will be removed after 2 hours from the end of the operation

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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