Outpatient Repair of Small Reducible Ventral Hernias Using Local Anesthesia: A Pilot Study
NCT07514273 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 35
Last updated 2026-04-07
Summary
Primary midline hernias, including umbilical and epigastric hernias, are prevalent surgical conditions, necessitating intervention. The optimal choice of anesthesia for umbilical and epigastric hernia repair remains an area of uncertainty. This pilot study focuses on the management of primary midline hernias, specifically umbilical and epigastric hernias, with an emphasis on anesthesia choice and repair techniques. Debates persist regarding the timing of elective repairs for primary ventral hernias. The study is prompted by the hypothesis that local anesthesia may offer superior outcomes, particularly for frail patients. While both mesh-reinforced and suture repairs are utilized, evidence supporting the superiority of mesh for small-sized hernias is limited.
A systematic review from 2017 supports the safety and feasibility of local anesthesia for umbilical hernia repair. A retrospective study indicates favorable outcomes, reduced operating time, and increased patient satisfaction with day case procedures under local anesthesia. This study aims to assess the safety and feasibility of repairing small reducible hernias using local anesthesia in the outpatient department. The investigation seeks to provide insights into the potential advantages of local anesthesia over general anesthesia in the repair of small reducible hernias. This summary succinctly outlines the key objectives, hypotheses, and methodologies of the pilot study within the specified word limit.
Conditions
- Ventral Hernia
Interventions
- PROCEDURE
-
Repair of small ventral hernia under lokal anesthesia
Outpatient Repair of Small Reducible Ventral Hernias Using Local Anesthesia: A Pilot Study
- PROCEDURE
-
Hernia Repair
Suture Repair of small size ventrla hernia with 2.0 Prolene suture
- PROCEDURE
-
OPD Repair
Hernia repair is performed in outpatient department (OPD) with local anaesthetics only, without ordinary operation theatre resources.
Sponsors & Collaborators
-
Region Örebro County
lead OTHER
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 80 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-01-01
- Primary Completion
- 2025-08-30
- Completion
- 2025-08-30
Countries
- Sweden
Study Locations
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