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Hernia, Hiatal clinical trials

View clinical trials related to Hernia, Hiatal.

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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: NCT04823767 Completed - Obesity, Morbid Clinical Trials

Single Anastomosis Sleeve Iejenal Bypass in Obese Patient With Hiatus Hernia

Start date: April 12, 2020
Phase: N/A
Study type: Interventional

single anastomosis sleeve jejunal bypass with hiatal repair for morbid obesity with reflux manifestations

NCT ID: NCT04716166 Completed - Cholecystitis Clinical Trials

Incentive Spirometry and Upper Abdominal Laparoscopic Surgery

Start date: October 1, 2020
Phase: N/A
Study type: Interventional

To compare the effects of volume-oriented versus flow-oriented incentive spirometry on pulmonary function tests and functional capacity in patients of upper abdominal laparoscopic surgery. Previous studies were designed to target only spirometer without focusing on its different types and their effects. This study covers the research gap and therefore is designed to observe effects of different types of spirometer on pulmonary function of patients undergoing upper abdominal laparoscopic surgery.

NCT ID: NCT04436159 Completed - Clinical trials for Gastro Esophageal Reflux

Partial Versus Total Fundoplication in the Surgical Repair of Para-esophageal Hernia.

Start date: May 1, 2009
Phase: N/A
Study type: Interventional

Short-term follow up after surgery of para-esophageal hernia comparing two different types of fundoplication

NCT ID: NCT04282720 Completed - Hiatal Hernia Clinical Trials

SurgiMend Mesh at the Hiatus

Start date: March 31, 2020
Phase: N/A
Study type: Interventional

Prospective, single-arm, open-label study to evaluate re-occurrence and quality of life in subjects undergoing primary Hiatal hernia repair using SurgiMend biological mesh. Up to 15, with a target of 10, subjects are planned to be enrolled at one site. All subjects will receive the SurgiMend mesh during surgery. Data collected will be compared to historical data. Subjects will complete a pre-operative visit. After surgery, in addition to any standard of care visits, subjects will complete 3- and 6-month follow-ups involving a phone QOL survey and will have an upper GI series at 6 months.

NCT ID: NCT04152798 Completed - Clinical trials for Gastroesophageal Reflux Disease

Approach to Hiatal Hernia Repair Based on Collagen Study

Start date: January 1, 2014
Phase: N/A
Study type: Interventional

Groups of patients who underwent laparoscopic repair of large hiatal hernias by primary posterior crural repair and crural repair with ProGrip™ mesh techniques were examined for recurrence rate of hiatal hernias, quality of life according to the GERD-HRQL questionnaire. Clinical evaluation was performed at 3, 6, 12, 24, 36, and 48 months after surgery.

NCT ID: NCT04007952 Completed - Clinical trials for Paraesophageal Hernia

Anterior Gastropexy vs. No Anterior Gastropexy for Paraesophageal Hernia Repair

Start date: June 26, 2019
Phase: N/A
Study type: Interventional

This study evaluates the effect of anterior gastropexy (one or more sutures fixing the stomach to the inner abdominal wall) on improving durability of paraesophageal hernia repair. Half of participants will receive anterior gastropexy, while the other half will not. The hypothesis is that anterior gastropexy will help to prevent paraesophageal hernias from recurring.

NCT ID: NCT03735862 Completed - Clinical trials for Gastroesophageal Reflux

Complications, Outcomes and Revisions Following Hiatal Hernia Repair With MIROMESH

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

Investigator will identify a consecutive cohort of patients who have undergone a hiatal hernia repair and are at least 6 months post index procedure.

NCT ID: NCT03730233 Completed - Hiatal Hernia Clinical Trials

Hiatal Hernia Repair by Tension-free Mesh Closure or Simple Suturing

Start date: January 11, 2006
Phase: N/A
Study type: Interventional

One-hundred and fifty-nine patients undergoing Nissen fundoplication for symptomatic gastro-oesophageal reflux disease (GORD), who had a concomitant hiatal hernia of > 2 cm axial length, were randomized to closure of the diaphragmatic hiatus with either crural sutures alone or tension-free closure with a non-absorbable mesh. Primary outcome variable was the incidence of radiologically verified recurrent hiatal hernia. Secondary outcomes were per-and postoperative complications and courses, symptomatic recurrence rate, use of PPI, postoperative oesophageal acid exposure and Quality of Life.

NCT ID: NCT03143608 Completed - Clinical trials for Gastro Esophageal Reflux

GERD Treatment With Transoral Incisionless Fundoplication (TIF) Following Hiatal Hernia Surgery

GERD
Start date: May 1, 2014
Phase: N/A
Study type: Observational [Patient Registry]

The investigators prospectively studied ninety nine GERD patients following laparoscopic hiatal surgery combined with transoral incisionless fundoplication at two community hospitals. General surgeons and gastroenterologists participated in the study. GERD questions were recorded before and at six and twelve months.