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Spinal Versus General Anesthesia for Laparoscopic Cholecystectomy

Spinal Versus General Anesthesia for Laparoscopic Cholecystectomy: a Cohort Study With Unselected Consecutive Patients

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02956252
Enrollment
1500
Registered
2016-11-07
Start date
2008-06-30
Completion date
2016-08-31
Last updated
2016-11-07

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

Conditions

Cholecystitis, Gallbladder Diseases

Keywords

cholecystectomy, laparoscopic, spinal anesthesia, general anesthesia, cholecystectomy

Brief summary

The aim of this study is to compare early postoperative outcomes of unselected consecutive patients underwent laparoscopic cholecystectomy (LC) under spinal versus general anesthesia.

Detailed description

Laparoscopic cholecystectomy (LC) is the gold standard surgical treatment of symptomatic cholecystectomy which traditionally performed under general anesthesia. Laparoscopy has provided many advantages over open surgery for the patients; however, general anesthesia adversely affects patients' early postoperative quality of life (POQoL). Spinal anesthesia which is a less invasive technique compared to general anesthesia has many advantages regarding the POQoL such as no need to wait for recovery from anesthesia, less nausea and vomiting, less or no pain at the end of surgery, no discomfort associated with intubation, early ambulation, fully awaken and oriented patient in the bed, and less anxious relatives. LC has been shown to be feasible under spinal anesthesia if performed with proper technique. There are many reports demonstrated the effectiveness and safety of LC under spinal anesthesia in selected patients. However, patients with complicated gallstone disease such as acute, gangrenous or subacute cholecystitis have been considered as unfit cases for LC under spinal anesthesia because of technical difficulties. On the other hand, spinal anesthesia has also been regarded as inappropriate for patients complying with American society for anesthesiology (ASA) III and IV due to the uncontrolled anesthesia risks. The aim of this study is to compare early postoperative outcomes of unselected consecutive patients underwent LC under spinal versus general anesthesia. If proportion of general anesthesia (PGA) / proportion of spinal anesthesia (PSA) denotes the proportion rate of outcomes in the general anesthesia group (GaG) / spinal anesthesia group (SaG), then two-sided test problem is assessed as follow: 1. Null hypothesis: H0: PGA = PSA. There is no difference between the two anesthesia techniques in terms of primary outcomes. 2. Null hypothesis: H1: PGA ≠ PSA There is a difference between the two anesthesia techniques in terms of primary outcomes.

Interventions

PROCEDURESpinal anesthesia

Spinal anesthesia was used in patients who underwent LC

PROCEDUREGeneral anesthesia

General anesthesia was used in patients who underwent LC

Sponsors

Zeugma Saglik Hizmetleri San. Tic. Ltd. Sti.
CollaboratorINDUSTRY
Medical Park Gaziantep Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* All patients who underwent laparoscopic cholecystectomy for symptomatic gallstone disease with no restriction for age, gender, ethnicity, disease severity, and ASA grade.

Exclusion criteria

* Patients were excluded if they underwent concurrent surgeries, had malignancy suspicion, received or converted to open surgery, and patients who were under spinal anesthesia converted to general anesthesia.

Design outcomes

Primary

MeasureTime frameDescription
Change in pain level for the first dayfrom baseline to postoperative 1, 2, 4 and 6 hoursNumerical rating scale (NRS) was used
Change in pain level for the first monthFrom postoperative 1 week to 1 monthNumerical rating scale was used

Secondary

MeasureTime frameDescription
Complicationswithin the postoperative 1 monthAll types of complications were assessed
Mortalitywithin the postoperative 1 monthall causes of mortality were recorded
Gastrointestinal quality of life indexchange from baseline to postoperative 1 week and 1 monthA standard form was used under the supervision of experienced independent personal
Patient satisfactionat postoperative 1 montha verbal or visual scale was used

Outcome results

None listed

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