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Ileostomy - Stoma clinical trials

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NCT ID: NCT03746353 Terminated - Colonic Neoplasms Clinical Trials

Early Closure Versus Conventional Closure in Postoperative Patients With Low Anteriresection for Rectal Cancer

Start date: September 5, 2018
Phase: N/A
Study type: Interventional

Colorectal cancer worldwide is the third most common in men and the second in female, although mortality is not as high as its incidence, there is less survival in developing countries. According to data from the World Health Organization, in 2012, there were an estimated 1.4 million cases and 693,900 deaths from this disease. Patients with rectal cancer are frequently taken to resection surgery as a curative management of their malignant pathology, according to the type of resection or reconstruction. In a high number of cases, they are management with colorectal anastomosis with a derivative ileostomy in the same procedure. The closure of this ileostomy is usually done after two to three months of the procedure, however in our environment it could take up to six or twelve months, during which time the patient is exposed to social difficulties, management problems and complications, derived from it. The early closure (7-12 days of its creation) of an ileostomy, despite the little evidence, seems to be a safe, feasible procedure that would save the patient having to live temporarily with an ileostomy.

NCT ID: NCT03707392 Recruiting - Ileostomy - Stoma Clinical Trials

A Randomized Trial of Inpatient Stoma-Nurse Teaching Versus Stoma Teaching Video Combined With Inpatient Stoma-Nurse Teaching

Start date: July 17, 2018
Phase: Phase 3
Study type: Interventional

Adult patients without prior history of ostomy, undergoing elective surgery involving a new ileostomy or colostomy will be randomized to receive standard ostomy nurse teaching or ostomy nurse teaching combined with preoperative and postoperative stoma care teaching video. Post operative outcomes including delay in discharge and stoma-related complications will be tracked.

NCT ID: NCT03703661 Enrolling by invitation - Clinical trials for Surgical Site Infection

Needle-Aspirated Compression Dressing Following Ostomy Reversal

Start date: August 27, 2017
Phase: Phase 3
Study type: Interventional

Negative pressure wound dressings have been studied and shown to have applications in decreasing rates of surgical wound infections. This study studies the effect of a low cost needle-aspirated negative pressure compression dressing on rates of wound infection at prior ostomy site in patients undergoing ostomy reversal surgery.

NCT ID: NCT03587519 Terminated - Ulcerative Colitis Clinical Trials

Short Versus Long Interval to Ileostomy Reversal After Ileal Pouch Surgery

SLIRPS
Start date: November 6, 2018
Phase: N/A
Study type: Interventional

In patients with ulcerative or indeterminate colitis who undergo ileal pouch anal anastomosis and diverting loop ileostomy (IPAA) surgery* a short interval to loop ileostomy reversal will result in differences in complications and quality of life compared to a long interval to loop ileostomy reversal.

NCT ID: NCT03549780 Recruiting - Ileostomy - Stoma Clinical Trials

Novel Stomal Occlusion Device in Patients With a Brooke Ileostomy

Start date: August 2, 2019
Phase: N/A
Study type: Interventional

This investigation constitutes an initial evaluation of the stoma occlusion device in humans with a mature permanent Brooke ileostomy. The overall objective of this study is to assess feasibility and initial operating characteristics of a novel stoma occlusion device. The study will recruit 20 patients for placement of the device into the mature Brooke ileostomy and subsequent 2 hour observation period. The device will remain in the ileostomy for up to 2 hours.

NCT ID: NCT03451253 Terminated - Clinical trials for Inflammatory Bowel Diseases

Effects of an Amino Acid Mixture on Gastrointestinal Function, Inflammation and Fluid Balance: A Pilot Study in Patients With Inflammatory Bowel Disease

Start date: April 12, 2018
Phase: N/A
Study type: Interventional

This pilot study will examine the benefit of this amino acid based hydration solution in patients with IBD who have undergone a total colectomy and have either ileostomies or jpouches. Findings from this study and possible future studies could have broad implications for patients with malabsorption resulting from many underlying conditions, including IBD.

NCT ID: NCT03439241 Completed - Ileostomy - Stoma Clinical Trials

Assessment of the Performance of a New Ostomy Device in Subjects Having an Ileostomy

Start date: February 5, 2018
Phase: N/A
Study type: Interventional

The purpose was to investigate the performance of a new ostomy device measured with a measuring device.

NCT ID: NCT03439176 Enrolling by invitation - Ileostomy - Stoma Clinical Trials

Investigating the Adhesion of New Adhesive to the Skin

Start date: January 15, 2018
Phase: N/A
Study type: Interventional

The adhesion of the new adhesive strips is investigated on healthy volunteers

NCT ID: NCT03427203 Completed - Ileostomy - Stoma Clinical Trials

Assessment of New Ostomy Devices in Subjects Having an Ileostomy

Start date: January 9, 2018
Phase: N/A
Study type: Interventional

The study investigates the performance of three new adhesives with regard to leakage and the skin condition.

NCT ID: NCT03424954 Terminated - Ileostomy - Stoma Clinical Trials

The Effect of a 30-day Automated Text Messaging Intervention on Hospital Based Acute Care Encounters Following Ileostomy

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

Each year a large number of patients undergo ileostomy surgery, a procedure in which a portion of the small intestine is attached to a hole in the abdominal wall, allowing for digested material to pass into a disposable bag worn attached to the skin. Ileostomies are performed for the treatment of a variety of diseases of the intestinal tract, such as inflammatory bowel disease, intestinal trauma, and gastrointestinal malignancy. Of the patients that undergo ileostomy surgery, 36% will require urgent medical care within the first 30 days of surgery. Most frequently, this is a result of dehydration due to excessive ostomy output. Thus, there is potential for significant improvement of the post-operative outcomes of ileostomy patients. Implementation of an automated text messaging system, EpxOstomy, can provide a way of monitoring patient's daily ostomy output and allow for timely intervention if output is outside normal limits, providing an effective way of improving patient outcomes while simultaneously reducing healthcare costs.