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Hernia clinical trials

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NCT ID: NCT04885140 Completed - Clinical trials for Lumbar Disc Herniation

Effect of Feedback Health Education on Postoperative Rehabilitation of Patients With Lumbar Disc Herniation

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

Aims and Objective: A theoretical model based on guided postoperative rehabilitation with feedback was developed for patients with lumbar intervertebral disc protrusion to explore the effects of feedback-based health education. Patients were assessed in terms of disease knowledge, general self-efficacy, medical behaviour, and the Oswestry disability index (ODI). During postoperative rehabilitation, nursing staff provided health education regarding lumbar intervertebral disc protrusion.

NCT ID: NCT04869046 Completed - Postoperative Pain Clinical Trials

Levobupivacaine and Postoperative Pain Relief

Start date: March 2013
Phase: Phase 4
Study type: Interventional

The study analysed direct levobupivacaine instillation in surgical wound and its effectiveness in postoperative pain control. Half participants received 0,5 % levobupivacaine and the other half received 0,9% saline solution

NCT ID: NCT04860609 Completed - Clinical trials for Lumbar Disc Herniation

Compare the Effects of Decompression on Lumber Disc Protrusion Patient

Start date: April 21, 2021
Phase: N/A
Study type: Interventional

This is an RCT study in which 60 participant are included and half of the participant are randomized via lottery method in control and experimental group after fulfilling the inclusion criteria. The sampling technique is convenient sampling . The study compare the effects of conventional Physical Therapy and Decompression Therapy and determine the effectiveness of Decompression as treatment procedure for patients with Lumbar disc protrusion. The data collection procedure included the NPRS, ODI, structural questionnaire and assesment on the 1st, 4th and 8th visit. Data will be analyzed on IBM SPSS-21 {Statistical Procedure of Social Sciences} software. The assessment will be done on 1st, 4th and 8th visits. after checking the normality of the date the Parametric/Non Parametric test will be apply to compare the means of the these groups. The 95% confidence interval will be used in term OD p value 0.05

NCT ID: NCT04853550 Completed - Ventral Hernia Clinical Trials

Long-Term Follow-up After Ventral Hernia Repair With Strattice Mesh

Start date: November 13, 2019
Phase:
Study type: Observational

This study will assess long-term outcomes (greater than 12 months) following ventral hernia repair with Strattice mesh reinforcement.

NCT ID: NCT04849403 Completed - Obesity, Morbid Clinical Trials

TROCAR SITE HERNIA AFTER LSG

Start date: January 1, 2015
Phase: N/A
Study type: Interventional

Today, laparoscopic sleeve gastrectomy (LSG) has become the most frequently performed bariatric surgical method. One of the complications seen after LSG is trocar site hernia (TSH). There is no clear information about the rate of TSH detected radiologically after LSG. Thick abdominal wall and failure to adequately expose the facial defect related to this, mobility limitations due to excessive subcutaneous fatty tissue are the reasons accused for increased incidence of TSH. Demographic characteristics and postoperative weight loss of patients who underwent LSG procedure in our clinic between January 2015 and June 2017 and whose facial defects in the trocar region were repaired with the Carter-Thomason Suture Passer (CTSP) were evaluated. TSH evaluation was made both by physical examination and superficial USG by a general surgeon who had radiological training on concurrent superficial abdominal ultrasonography (USG). Detected TSHs were divided into two groups as symptomatic and asymptomatic.

NCT ID: NCT04839848 Completed - Chronic Pain Clinical Trials

Chronic Postoperative Pain After the Lichtenstein Groin Hernioplasty

Start date: September 1, 2012
Phase:
Study type: Observational [Patient Registry]

The study attempts to quantify the relative risks for chronic postoperative inguinal pain (CPIP) after Lichtenstein repair of groin hernia, depending on mesh type and fixation suture material. For this purpose the investigators will analyze data from the Swedish Hernia Registry (SHR).

NCT ID: NCT04838028 Completed - Chronic Pain Clinical Trials

Chronic Postoperative Pain After Laparoscopic Groin Hernia Repair

Start date: September 1, 2012
Phase:
Study type: Observational

The study attempts to quantify the relative risks for chronic postoperative inguinal pain (CPIP) depending on different combinations of mesh and mesh fixation. For this purpose the investigators will analyze data from the Swedish Hernia Registry (SHR).

NCT ID: NCT04806828 Completed - Inguinal Hernia Clinical Trials

Preoperative Score of Inguinal Hernias. Is it Useful to Predict Outcomes

POINTHER
Start date: January 1, 2019
Phase:
Study type: Observational [Patient Registry]

To analyze and validate a preoperative score of difficulty of inguinal hernias and its correlation with postoperative outcomes

NCT ID: NCT04801394 Completed - Incisional Hernia Clinical Trials

Retrospective Analysis on Large Incisional Hernia in High Risk Patients

Start date: April 1, 2010
Phase: N/A
Study type: Interventional

Large incisional hernia (LIH) is a challenging condition where the abdominal wall is hopelessly compromised. Nowadays the best treatment option in this particularly frail subset of patients is a major issue. The Auhtors proposed the clinical experience with an innovative approach with the composite Free Lateral Polypropylene prosthesis (FLaPp®) mesh fashioned as "neoperitoneum" analyzing its feasibility and short/medium term results.

NCT ID: NCT04793009 Completed - Hernia Clinical Trials

Prophylactic Funnel Mesh to Prevent Parastomal Hernia in Permanent End Colostomy After Abdomino-perineal Resection

Start date: January 1, 2013
Phase:
Study type: Observational

This retrospective study asses if a prophylactic, funnel-shaped, intraperitoneal mesh prevents parastomal hernia in patients undergoing abdominoperineal rectum resection with permanent end colostomy.