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Clinical Trials/NCT05822882
NCT05822882
Completed
Not Applicable

Efficacy of Postoperative Epidural Anesthesia Following Abdominoplasty

Klinik Bogenhausen1 site in 1 country112 target enrollmentDecember 14, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Anesthesia
Sponsor
Klinik Bogenhausen
Enrollment
112
Locations
1
Primary Endpoint
frequency of retrieval of the on-demand non-epidural opiate
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

Effective postoperative pain management is essential for patient satisfaction and therefore intraoperative regional nerve blocks have become more and more popular in abdominoplasties. However, the key disadvantage of these blocks are their limited duration of action. This observational study evaluates the effects of a longer- lasting, individualized epidural analgesia using a pain pump to better classify the clinical value of this procedure.

Detailed Description

This work reviews the digital medical charts of patients who underwent selective abdominoplasty without additive surgical procedures within a period of 4 years. Evaluated data comprise the postoperative analgesia regimen, including on-demand medication, mobilization time, inpatient length of stay, and clinical outcome. The patients were grouped by the presence of an epidural catheter.

Registry
clinicaltrials.gov
Start Date
December 14, 2022
End Date
February 24, 2023
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Klinik Bogenhausen
Responsible Party
Principal Investigator
Principal Investigator

Ulf Dornseifer, MD

Principal Investigator

ISAR Klinikum

Eligibility Criteria

Inclusion Criteria

  • Patients who underwent abdominoplasty

Exclusion Criteria

  • Patients who underwent abdominoplasty combined with additional intraoperative procedures (e.g., liposuction, hernia repair) were excluded

Outcomes

Primary Outcomes

frequency of retrieval of the on-demand non-epidural opiate

Time Frame: from the day of inpatient admission to the day of discharge of every included patient. The event determined by reviewing digital medical charts, is therefore assessed for an estimated period of up to 7 days

frequency of retrieval of the on-demand non-epidural opiate as a measure of perceived pain discomfort

Secondary Outcomes

  • postoperative mobilization ability(from the day of inpatient admission to the day of discharge of every included patient. The event determined by reviewing digital medical charts, is therefore assessed for an estimated period of up to 7 days)
  • timing of urinary catheter removal(from the day of inpatient admission to the day of discharge of every included patient. The event determined by reviewing digital medical charts, is therefore assessed for an estimated period of up to 7 days)
  • length of hospital stay(from the day of inpatient admission to the day of discharge of every included patient. The event determined by reviewing digital medical charts, is therefore assessed for an estimated period of up to 7 days)

Study Sites (1)

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