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Efficacy of Postoperative Epidural Anesthesia Following Abdominoplasty

Efficacy of Postoperative Epidural Anesthesia Following Abdominoplasty

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05822882
Acronym
EDA
Enrollment
112
Registered
2023-04-21
Start date
2022-12-14
Completion date
2023-02-24
Last updated
2023-04-21

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

Conditions

Abdominoplasty, Anesthesia

Keywords

abdominoplasty, postoperative analgesia, regional anesthesia, epidural anesthesia, epidural catheter

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.

Interventions

PROCEDUREEpidural anesthesia

Postoperative pain management by epidural anesthesia via epidural catheter and pain pump

Sponsors

ISAR Klinikum
CollaboratorOTHER
Klinik Bogenhausen
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

• Patients who underwent abdominoplasty

Exclusion criteria

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

Design outcomes

Primary

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

Secondary

MeasureTime frameDescription
postoperative mobilization abilityfrom 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 daysthe time at which the patient was able to move at room level with the assistance of a nurse (assisted full mobilization), the time at which the patient was able to get out of bed independently and move without assistance (independent full mobilization)
timing of urinary catheter removalfrom 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 daystiming of urinary catheter removal after surgery
length of hospital stayfrom 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 daysnumber of days from the day of surgery until dischargement

Countries

Germany

Outcome results

None listed

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