Effect of Inguinal Hernia Repair on Isokinetic Muscle Strength
- Conditions
- Inguinal Hernia
- Interventions
- Procedure: KugelProcedure: 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
- 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
- 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
Group Intervention Description Kugel Kugel Kugel procedure lichtenstein lichtenstein lichtenstein procedure
- Primary Outcome Measures
Name Time Method isokinetic muscle strength 6 - 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
Name Time Method quality of life assesment 6 -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