CompletedNot Applicable

ISOperistaltic Versus ANTIperistaltic Anastomosis After Laparoscopic Right Colectomy for Cancer

Spain108 participantsStarted 2014-06

Plain-language summary

The study will provide a precise control compared to the two interventions (iso vs antiperistaltic anastomoses) with thorough measurements of the postoperative variables and complications to improve the evaluation of the surgical technique. It will also enable an evaluation of the quality of life after the procedures.

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * The patient has given informed consent to participate * No surgery contraindications * Elective surgery * No pregnancy or nursery during the study * Older than 18 years * Complete preoperative cancer staging * Tumour characteristics: * Cecum, ascending, hepatic angle or transverse colon tumour confirmed by endoscopic biopsy * Radiologically resectable tumours * Absence of vascular, nervous or bone infiltration * T4 stages with near organ infiltration * Absence of peritoneal carcinomatosis * Absence of respiratory pathology that prevents for doing hydrogen breath test Exclusion Criteria: * Pregnancy * Intestinal bowel disease like Crohn's disease or ulcerative colitis. * Metastatic bone illness * Previous abdominal surgery with bowel resection * Malabsorption syndromes

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

postoperative complications

Timeframe: within the first 30 days up to one year after surgery

Trial details

NCT IDNCT02309931

SponsorHospital Universitario Virgen de la Arrixaca

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2016-11-01

View on ClinicalTrials.gov More Primary Malignant Neoplasm of Ascending Colon trials