Retrospective Analysis of the Geriatric Patients Underwent Unilateral Inguinal Herniorrhaphy

NCT ID: NCT02418078

Last Updated: 2015-04-16

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

370 participants

Study Classification

OBSERVATIONAL

Study Start Date

2015-02-28

Study Completion Date

2015-03-31

Brief Summary

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The aim of this study is to compare the geriatric patients with the non-geriatrics undergoing outpatient unilateral herniorrhapy in terms of local anesthesia, sedation, recovery and early morbidity.

Detailed Description

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A retrospective data analysis will be conducted and the patient records will be evaluated for patient characteristics local anesthesia, sedation, recovery and early morbidity.

Conditions

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Inguinal Hernia

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

RETROSPECTIVE

Study Groups

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Geriatri

patients ageing ≥ 65 yr undergoing herniorrhaphy with local infiltration anesthesia and sedation

local infiltration anesthesia and sedation

Intervention Type PROCEDURE

the surgical site is infiltrated with local anesthetic agents and the patients are sedated with intravenous agents

non-geriatri

patients ageing 19-64 yr undergoing herniorrhaphy with local infiltration anesthesia and sedation

local infiltration anesthesia and sedation

Intervention Type PROCEDURE

the surgical site is infiltrated with local anesthetic agents and the patients are sedated with intravenous agents

Interventions

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local infiltration anesthesia and sedation

the surgical site is infiltrated with local anesthetic agents and the patients are sedated with intravenous agents

Intervention Type PROCEDURE

Other Intervention Names

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local anesthesia and sedation

Eligibility Criteria

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Inclusion Criteria

patients with a unilateral inguinal hernia undergoing herniorrhaphy

Exclusion Criteria

none
Minimum Eligible Age

19 Years

Maximum Eligible Age

90 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Diskapi Teaching and Research Hospital

OTHER

Sponsor Role lead

Responsible Party

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DILEK YAZICIOGLU

DR

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Hakan Kulacoglu, Prof

Role: STUDY_DIRECTOR

Diskapi Teaching and Research Hospital

Locations

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Dıskapı TRH

Ankara, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

References

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Mattila K, Hynynen M; Intensium Consortium Study Group. Day surgery in Finland: a prospective cohort study of 14 day-surgery units. Acta Anaesthesiol Scand. 2009 Apr;53(4):455-63. doi: 10.1111/j.1399-6576.2008.01895.x. Epub 2009 Feb 23.

Reference Type RESULT
PMID: 19239413 (View on PubMed)

Majholm B, Engbaek J, Bartholdy J, Oerding H, Ahlburg P, Ulrik AM, Bill L, Langfrits CS, Moller AM. Is day surgery safe? A Danish multicentre study of morbidity after 57,709 day surgery procedures. Acta Anaesthesiol Scand. 2012 Mar;56(3):323-31. doi: 10.1111/j.1399-6576.2011.02631.x.

Reference Type RESULT
PMID: 22335277 (View on PubMed)

Dallas KB, Froylich D, Choi JJ, Rosa JH, Lo C, Colon MJ, Telem DA, Divino CM. Laparoscopic versus open inguinal hernia repair in octogenarians: a follow-up study. Geriatr Gerontol Int. 2013 Apr;13(2):329-33. doi: 10.1111/j.1447-0594.2012.00902.x. Epub 2012 Jun 21.

Reference Type RESULT
PMID: 22726915 (View on PubMed)

Other Identifiers

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Geriatri Hernia

Identifier Type: -

Identifier Source: org_study_id

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