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Mesh Hernioplasty Of Strangulated Hernias With Intestinal Resection

Mesh Hernioplasty Of Strangulated Hernias With Intestinal Resection

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01411397
Enrollment
163
Registered
2011-08-08
Start date
2005-06-30
Completion date
2011-01-31
Last updated
2011-08-08

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

Conditions

Strangulated Hernia

Keywords

Infection, Prosthesis, Recurrence, Strangulation

Brief summary

Primary suture repair increases the risk for recurrence, the fact of benefit of mesh repair in elective situations is documented, and many studies have reported beneficial outcomes of mesh hernioplasty in emergency situations. Still there is controversy of using such grafts in presence of intestinal resection.

Detailed description

Patients with acutely incarcerated hernias (with small intestine contents) who underwent polypropylene mesh hernioplasty were included in this prospective study from June 2005 through Jan. 2011, patients were categorized into 2 groups who required intestinal resection anastomosis (group I)or not (group II).

Interventions

mesh repair of strangulated hernia without resection

OTHERSURGERY

REPAIR OF STRANGULATED HERNIA with intestinal resection

Sponsors

Mansoura University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

* strangulated hernias

Exclusion criteria

* above 75, under 18 * recurrent hernia * peritonitis * pure omentum contents ASA above 3

Design outcomes

Primary

MeasureTime frame
wound infection5 weeks

Secondary

MeasureTime frameDescription
operative time3hoursthe time from skin incision up to skin closure
morbidity5 monthsthe perioperative complications
recurrence of the hernia6monthsRecurrence of the hernia was defined as an apparent swelling or a palpable defect at the previous surgery site detected clinically or radiologically by ultrasound if needed

Countries

Egypt

Outcome results

None listed

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