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Hernia clinical trials

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NCT ID: NCT05296200 Completed - Clinical trials for Intervertebral Disc Herniation

Cervical Changes by 4h of Hyper-buoyancy Flotation and Followed by 15 Mins 1g Re-loading

Start date: March 13, 2020
Phase:
Study type: Observational

Study with the aim to see the effect on a space ground anaologue, Hyperbuoyancy Floatation (HBF) on cervical column.

NCT ID: NCT05288634 Completed - Clinical trials for Lumbar Disc Herniation

The Effect of Progressive Relaxation Exercise on Pain and Kinesiophobia After Lumbar Disc Herniation Surgery

Start date: March 14, 2022
Phase: N/A
Study type: Interventional

We aimed to assess the influence of progressive muscle relaxation exercise on kinesiophobia and pain during after lumbar disc surgery using the Visual Analog Scale (VAS) and the Tampa Kinesiophobia Scale in a prospective, randomized fashion.

NCT ID: NCT05261815 Completed - Clinical trials for Disk Herniated Lumbar

Compare Effects of Ultrasound Therapy With High Intensity Laser Therapy for Treatment of Lumbar Disc Herniation.

Start date: March 1, 2021
Phase: N/A
Study type: Interventional

The aim of this study is to assess and compare the effects of ultrasound therapy and High Intensity Laser Therapy, as the treatment option in case of lumbar disc herniation.

NCT ID: NCT05251350 Completed - Clinical trials for Incarcerated Inguinal Hernia

Incarcerated Right Inguinal Hernia Containing Sigmoid Colon: An Unusual Case Report

Start date: September 10, 2021
Phase:
Study type: Observational

Incarcerated inguinal hernia is an irreducible but the blood supply to the contained part is intact, but developing towards strangulation. Here the lumen of the portion of colon occupying a hernia sac is blocked with faeces.

NCT ID: NCT05247983 Completed - Clinical trials for Inguinal Hernia, Without Mention of Obstruction or Gangrene

Tension-free Repair of Inguinal Hernia With "Undissociate Spermatic Cord"

Start date: March 1, 2014
Phase:
Study type: Observational

The theory of "undissected Spermatic cord (US)" only transected the hernia ring ends in the abdominal cavity, the hernia ring, hernia sac and spermatic cord will not be dissected. Its significance lies in that inguinal hernia repair can get rid of the "entanglement" of hernia sac and spermatic cord and fundamentally change the treatment mode of hernia ring and hernia sac.

NCT ID: NCT05246241 Completed - Clinical trials for Lumbar Disc Herniation

Preoperative Magnetic Resonance Imaging Abnormalities Predictive of Lumbar Herniation Recurrence

Start date: April 1, 2021
Phase:
Study type: Observational

There are currently no standard criteria for evaluating the risk of recurrent disk herniation following surgical repair. This study investigated the predictive values of five presurgical imaging parameters, paraspinal muscle quality, annular tear size, Modic changes, modified Pfirrmann's disc degeneration grade, and presence of sacralization or fusion. Clinical status and MRI findings were evaluated before surgery and 4, 12, and 24 months post-surgery using a Visual Analog Scale (VAS), Oswestry Disability Index (ODI), and Short Form 36 (SF36).

NCT ID: NCT05245214 Completed - Clinical trials for Disk Herniated Lumbar

Muscle Analyze In Patient With Disc Herniation

Start date: March 2, 2021
Phase:
Study type: Observational

This study which was planned to investigate the factors affecting m. erector spinae (ES), m. multifidus (MF), m. psoas major (PM) and m. quadratus lumborum (QL), which stabilize the lumbar region in the case of disc herniation. In this study, the effects of disc herniation, herniation severity, age, and spinal biomechanics were investigated.

NCT ID: NCT05238571 Completed - Clinical trials for Patients With Persistent Severe Pain After Groin Hernia Repair

Does Re-surgery Improve Somatosensory Outcomes in Persistent Pain After Groin Hernia Repair

Start date: April 24, 2009
Phase:
Study type: Observational

Groin hernia repair is accompanied by persistent severe pain in 2-4% of the patients significantly restraining psychophysical functions. Re-surgery with meshectomy and selective neurectomy may improve the pain condition, compared to non-surgical alternatives. In the current study, the primary objective was to examine and describe the underlying pathophysiological perturbations by quantitative somatosensory testing before and after re-surgery.

NCT ID: NCT05234840 Completed - PRP Clinical Trials

"Platelet-Rich Plasma" Epidural Injection an Emerging Strategy in Lumbar Disc Herniation

Start date: April 1, 2019
Phase: N/A
Study type: Interventional

To evaluate the efficacy of platelet-rich plasma (PRP; double-spin) in treatment of single-level lumbar herniated nucleus pulposus (HNP) in comparison to triamcinolone. RCT was conducted with 30 patients included.

NCT ID: NCT05234242 Completed - Clinical trials for Outcome of Outpatient/Ambulatory and Inpatient/Stationary Setting

Inguinal Hernia Treatment: Stationary/Inpatient vs. Ambulatory/Outpatient Setting - HerStAmb Study

Start date: January 1, 2019
Phase:
Study type: Observational

Since 01/2018, AVOS (ambulant vor stationär = ambulatory to stationary) regulation has been progressively implemented in hospitals across Switzerland for certain surgical procedures, including the treatment of inguinal hernias. The aim of this prospective, non-randomized, multicenter study was to compare the outcome of outpatient/ambulatory and inpatient/stationary postoperative care by examining the re-admission rate, complication rate and quality of life in patients with primary unilateral inguinal hernia repair.