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Clinical Trials/NCT02768376
NCT02768376
Unknown
Not Applicable

Spinal for Laparoscopic Cholecystectomy

Mansoura University1 site in 1 country60 target enrollmentMarch 2016

Overview

Phase
Not Applicable
Intervention
General anesthesia
Conditions
Laparoscopic Cholecystectomy
Sponsor
Mansoura University
Enrollment
60
Locations
1
Primary Endpoint
Patient satisfaction (over a scale from 1 to 4)
Last Updated
9 years ago

Overview

Brief Summary

In this study, the investigators will study spinal anesthesia for laparoscopic cholecystectomy in comparison to general anesthesia (GA) regarding patient satisfaction as a primary variable, intraoperative complications, postoperative analgesic requirements, postoperative nausea and vomiting, patient hospital stay (secondary variables).

Registry
clinicaltrials.gov
Start Date
March 2016
End Date
October 2017
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

AlRefaey Kandeel

Dr

Mansoura University

Eligibility Criteria

Inclusion Criteria

  • patients scheduled for laparoscopic cholecystectomy

Exclusion Criteria

  • coagulopathy
  • Patient refusal
  • previous spine surgery
  • Obesity BMI more than 30

Arms & Interventions

General anesthesia group

General anesthesia group: Standard anesthetic technique will be applied.Anesthesia will be induced by propofol 1% (1-2 mg/kg), Fentanyl 1-2 mic/kg, and Atracurium 0.5 mg/kg then according to train of four response. Then maintained using Sevoflurane based anesthesia aiming to maintain Bispectral index 40-60..

Intervention: General anesthesia

Spinal anesthesia group

While in sitting position; intrathecal injection using 25 G spinal needle using 3 mls of Bupivacaine 0.5% with 20 mic Fentanyl, at L 2-3 level the patient head will be lowered till sensory blockade of T6 obtained at least.

Intervention: Bupivacaine with Fentanyl (Spinal Anesthesia)

Outcomes

Primary Outcomes

Patient satisfaction (over a scale from 1 to 4)

Time Frame: 24 hours

Postoperative analgesic consumption (mg morphine)

Time Frame: 24 hours

Study Sites (1)

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