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Hernia clinical trials

View clinical trials related to Hernia.

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NCT ID: NCT05136534 Completed - Hernia, Inguinal Clinical Trials

Spinal Versus Local Anesthesia for Hernia Repair

SPINOFAST
Start date: January 10, 2019
Phase: N/A
Study type: Interventional

patients underwent inguinal hernia repair; Group A patients received Subarachnoid anesthesia; Group B Patients underwent surgery with local anesthesia (Mepivacaine 2%) performed by the surgeon; Pain assessment was performed using a 0-10 Numerical Rating Scale (NRS). Intraoperative pain was assessed every 10 minutes,

NCT ID: NCT05122351 Completed - Clinical trials for Analgesia in Patients With Open Inguinal Hernia Surgeries

Comparative Study Between The Efficacy Of Quadratus Lumborum Block VS Conventional Analgesia In Patients Undergoing Open Inguinal Hernia Surgical Repair

Start date: October 1, 2021
Phase: Early Phase 1
Study type: Interventional

Analgesia In Patients Undergoing Open Inguinal Hernia Surgical Repair

NCT ID: NCT05121467 Completed - Clinical trials for Cervical Disc Herniation

Muscular Endurance And Its Association With Neck Pain, Disability, Neck Awareness, And Kinesiophobia

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

The aim of this study was to investigate the relationship of muscular endurance of the trunk, upper extremities, and scapular region as well as cervical region, with pain, neck awareness, and kinesiophobia in patients with cervical disc herniation. Thirty-six patients between 18-65 years with a diagnosis of cervical disc herniation and having neck pain of 2 and above at rest according to the Visual Analogue Scale (VAS) were included in the study. After the evaluation of musculoskeletal system, endurance tests were performed for 9 muscles/muscle groups in the cervical and scapular regions, upper limb, and trunk. Pain severity was measured by VAS and Neck Disability Index (NDI), neck awareness with Fremantle Neck Awareness Questionnaire (FreNAQ), and fear of movement with Tampa Kinesiophobia Scale (TKS).

NCT ID: NCT05107986 Completed - Inguinal Hernia Clinical Trials

Laparoscopy in Complicated Groin Hernia

Start date: September 1, 2017
Phase:
Study type: Observational

This study assessed the outcomes of laparoscopic repair in complicated groin hernia. Laparoscopic approach in cases of complicated groin hernia can achieve desirable patient outcomes without major complications, provided good patient selection and expertise. This study provides an insight to the outcomes from the procedure in low resource setting of Nepal.

NCT ID: NCT05073055 Completed - Postoperative Pain Clinical Trials

Spinal Anesthesia Versus Erector Spina Plane Block

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

The primary aim of our study was to use spinal anesthesia for unilateral inguinal hernia surgery and lumbar erector spina block supported by local infiltration anesthesia in terms of operation time, intraoperative hemodynamic data, motor block onset time, block termination time, analgesic need, discharge time, patient satisfaction, surgeon satisfaction. is to compare. Its second purpose is to observe nausea, vomiting, urinary retention, headache, chills, bleeding, wound infection.

NCT ID: NCT05069493 Completed - Quality of Life Clinical Trials

Long-term Follow-up After Hiatal Hernia Repair by Tension-free Mesh Closure or Simple Suturing

Start date: September 15, 2021
Phase:
Study type: Observational

10 years of follow-up after surgery for hiatal hernia by tension-free mesh closure or simple suturing.

NCT ID: NCT05069142 Completed - Inguinal Hernia Clinical Trials

Peri-Operative Rehab Program for Inguinal Hernia Repair Surgery

Start date: January 1, 2022
Phase: N/A
Study type: Interventional

Inguinal hernia repair is one of the most common surgeries, with more than 20 million performed globally each year. It is estimated that approximately 15% of patients undergoing inguinal hernia repair will experience persistent post-surgical pain that could last months to years. Evidence from related procedures indicates that better surgical preparation through pre-operative exercise and education (i.e. Prehabilitation) followed by ongoing post-surgical rehabilitation leads to more rapid recovery, return to activities and lower likelihood of persistent post-surgical pain. The investigators will determine the feasibility of a peri-operative rehabilitation program (pre- and post-surgery) and our study protocol for patients undergoing inguinal hernia repair surgery. The investigators hypothesize that: 1) our peri-operative intervention will be feasible and safe to undertake within a clinical setting; 2) adequate numbers will be enrolled to justify a larger trial; and that 3) our outcome measurement protocol will provide meaningful information with high response rate and low attrition after 3 months.

NCT ID: NCT05061264 Completed - Infection Clinical Trials

Abdominal Wall Reconstruction With PVDF Mesh in the Setting of Active Infection

Start date: May 2016
Phase: N/A
Study type: Interventional

The use of synthetic mesh to repair infected defects of the abdominal wall remains controversial. This study aimed to evaluate the short-term outcomes of using PVDF mesh to treat infected abdominal wall defects in the elective setting.

NCT ID: NCT05021718 Completed - Clinical trials for Lumbar Disc Herniation

Strengthening Exercise and Activities of Daily Living Instructions for Patients With Lumbar Disc Herniation

Start date: July 1, 2018
Phase: N/A
Study type: Interventional

Lumbar disc herniation (LDH) is one of the most common causes of mechanical low back pain (LBP) associated with radiating leg pain. Conservative treatment, including exercise, analgesic, and physical therapy, is regarded as the first-line treatment of LDH. This randomized clinical trial was conducted to evaluate the effectiveness of back and hip strengthening exercises combined with activities of daily living instructions (ADLIs) to reduce pain intensity in patients with LDH.

NCT ID: NCT05011786 Completed - Inguinal Hernia Clinical Trials

Open and Laparoscopic Hernia Repair. A Comparative Study

Start date: January 1, 2017
Phase:
Study type: Observational

A retrospective comparative study in a pediatric surgery center to compare the outcomes of 2 approaches of hernia repair in the pediatric population.