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Effect of Inguinal Hernia Repair on Isokinetic Muscle Strength

Not Applicable
Completed
Conditions
Inguinal Hernia
Interventions
Procedure: Kugel
Procedure: lichtenstein
Registration Number
NCT02871583
Lead Sponsor
Konya Meram State Hospital
Brief Summary

The aim of the present prospective controlled study is to compare the trunk muscle strength, quality of life and neuropathic pain component after Lichtenstein and Kugel procedures.

Detailed Description

In this study patients underwent inguinal hernia repair will be evaluated for the effect of the surgical procedure on abdominal muscle strength.

Recruitment & Eligibility

Status
COMPLETED
Sex
Male
Target Recruitment
100
Inclusion Criteria
  • Signed written informed consent
  • Male gender (for minimizing the certain effect of gender to muscle strength)
  • Patients aged 18-65 years' old
  • Having no previous surgery
  • Patients within six months to postoperative first year
  • Ability to speak, read, and write Turkish
Exclusion Criteria
  • Infections or tumors of the spine
  • Systemic bone or joint disorders (e.g., rheumatoid arthritis)
  • Unstable cardiovascular and pulmonary diseases
  • Polyneuropathies and musculoskeletal system diseases
  • Presence of a diagnosed severe psychiatric disorder
  • Presence of severe pain
  • Regular exercise habit
  • Recurrent operation for a hernia
  • Presence bilateral inguinal hernia on concurrent femoral hernia
  • If the calculated Body mass index is lower than 20kg/cm2 or over than 35kg/cm2

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
KugelKugelKugel procedure
lichtensteinlichtensteinlichtenstein procedure
Primary Outcome Measures
NameTimeMethod
isokinetic muscle strength6 - 12 months

Trunk muscle strength measurement using the Biodex System 3Pro Multi-joint System Isokinetic dynamometer. Peak torque (PT) and PT-based agonist/antagonist ratios will be used to reveal strength imbalances.

Secondary Outcome Measures
NameTimeMethod
quality of life assesment6 -12 months

Quality of life assesment will be performed by Short Form 36 (SF-36) and The PainDETECT questionnaires (PD-Q).

Trial Locations

Locations (1)

Konya Training and Research Hospital

🇹🇷

Konya, Turkey

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