Efferent loop stimulation before ileostomy closure
Implementation of an Efferent Loop Stimulation Protocol Prior to Ileostomy Closure at La Paz University Hospital
This study is testing if stimulating a part of the intestine with a special solution before closing an ileostomy can help patients recover better and have fewer complications after surgery.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 68 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Hospital Universitario La Paz Academic / other |
| Locations | 1 site (Madrid) |
| Trial ID | NCT06974500 on ClinicalTrials.gov |
What this trial studies
This study aims to implement a protocol for stimulating the efferent limb of the intestine prior to the closure of ileostomies at Hospital Universitario La Paz. The intervention involves daily stimulation using a saline solution and thickening agent for at least two weeks before surgery. The goal is to improve postoperative recovery outcomes, reduce complications, and enhance the quality of life for patients undergoing ileostomy closure. By establishing a formal protocol, the study seeks to provide a structured approach to this intervention, which has shown potential benefits in previous research.
Who should consider this trial
Good fit: Ideal candidates are adults over 18 years old with a medical indication for intestinal reconstruction and an existing ileostomy.
Not a fit: Patients who do not wish to undergo intestinal reconstruction or cannot complete the required stimulation period will not benefit from this study.
Why it matters
Potential benefit: If successful, this protocol could significantly improve postoperative recovery and quality of life for patients with temporary ileostomies.
How similar studies have performed: Previous studies have indicated benefits from similar stimulation approaches, suggesting potential for success in this protocol.
Eligibility criteria
Show full inclusion / exclusion criteria
IInclusion Criteria: 1. Subjects must be able to understand the purpose and risks of the study, provide informed consent, and authorise the use of confidential health information. 2. Patients over 18 years of age who, regardless of the underlying cause, have an ileostomy and a medical indication for intestinal transit reconstruction by a general surgeon. 3. Subjects who are able and willing to participate and to comply with follow-up for the duration of the study. Exclusion Criteria: 1. Subjects with an ileostomy who do not wish to undergo intestinal reconstruction. 2. Subjects who are unable to complete at least two weeks of efferent loop stimulation prior to reconstruction surgery. 3. Subjects who do not provide consent to participate in the study.
Where this trial is running
Madrid
- Hospital Universitario La Paz — Madrid, Spain (Recruiting)
Study contacts
- Principal investigator: Luis Asensio, Consultant — Hospital Universitario La Paz
- Study coordinator: Luis Dr. Asensio Gómez, Consultant
- Email: lasensio@salud.madrid.org
- Phone: +34 650675894
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.