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Enhanced Recovery After Lumber Laminectomy Using Epidural and General Anesthesia

NCT04981158 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2023-08-18

No results posted yet for this study

Summary

Now, enhanced recovery after surgery (ERAS) is considered an essential goal to improve patient satisfaction, increase surgical workflow rate and facilitate performing different surgical procedures, including lumber laminectomy, on an ambulatory base. Different ERAS protocols have been applied and succeeded to improve recovery profile after colonic, rectal, gastric, urologic, biliary, pancreatic, and gynecologic procedures. Up to our knowledge, it is the 1st trial that will investigate the effect of combining single shot epidural blockade and general anesthesia (GA) using tolerable endotracheal tube (TET), as components for ERAS protocol for patients undergoing lumber laminectomy, on postoperative recovery profile. so the current study will be done to assess if Single shot epidural blockade and GA using TET, for patients undergoing lumber laminectomy, can enhance their postoperative recovery.

Conditions

  • Postoperative Recovery
  • Epidural Blockade
  • Endotracheal Tube
  • Laminectomy

Interventions

PROCEDURE

(Epidural /GA using tolerable endotracheal tube (TET) group, group II

patients will undergo a single shot epidural bupivacaine (15 ml with 0.25% concentration) followed by a standard general anesthetic technique in which the trachea was intubated using TET, through its side port 2mg/kg , lidocaine 2% will be sprayed immediately after intubation when the patient is in flat supine position then the same dose of lidocaine will be repeated 10 minutes before anesthetic discontinuation.

PROCEDURE

standard general anesthetic technique, control group, group I

patients will undergo standard general anesthesia with classic endotracheal tube

Sponsors & Collaborators

  • Zagazig University

    lead OTHER_GOV

Principal Investigators

  • tarek Y Gaafar, MD · Zagazig University

  • abeer M elnakera, MD · Zagazig University

  • abeer H alsawy · Zagazig University

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-01-15
Primary Completion
2017-12-12
Completion
2018-04-20

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04981158 on ClinicalTrials.gov