Perioperative Safety and Long-Term Outcomes of Mesh Repair in Nonagenarians Undergoing Elective Inguinal Hernia Repair

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age90+
SponsorFudan University

About this trial

To evaluate the clinical characteristics, postoperative outcomes, and factors associated with Clavien-Dindo grade ≥II complications in nonagenarians undergoing elective inguinal hernia repair. Preoperative, intraoperative, and postoperative data of nonagenarians who underwent elective inguinal hernia repair were collected. The primary outcome was Clavien-Dindo grade ≥II complications. Univariable logistic regression was used to identify associated factors.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial population

Patients aged 90 years or older who underwent elective inguinal hernia repair

Trial design

Design model

Cohort

Time perspective

Retrospective

Treatments tested in this trial

Not listed

Trial groups

150 Participants
are grouped into 1 trial group
Group A: nonagenarians

Trial outcomes

Primary outcomes

1

Clavien-Dindo grade ≥II complications

The Clavien-Dindo classification grades complications according to the intensity of treatment required. Grade II or higher complications generally include events requiring pharmacologic therapy, interventional treatment, surgery, or resulting in death.

Time frame
30 days

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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