Skip to content

RISE Ileocecal Valve Functional Reconstruction

RISE Ileocecal Valve Functional Reconstruction for the Prevention of Postoperative Intestinal Dysfunction After Robotic/Laparoscopic Right Hemicolectomy: a Single-blind, Two-arm, Multicenter Randomized Controlled Clinical Study

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07167420
Enrollment
188
Registered
2025-09-11
Start date
2025-10-01
Completion date
2028-10-01
Last updated
2025-09-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Right-sided Colon Cancer

Keywords

right-sided colon cancer, laparoscopic surgery, ileocecal valve

Brief summary

The traditional surgical treatment for right-sided colon cancer involves the removal of an important structure, the ileocecal valve, which includes the ileocecal valve. This can lead to problems such as diarrhea and malnutrition in patients. This study reconstructs an artificial ileocecal valve through intraoperative suturing to compensate for the function of the original ileocecal valve. The control group will undergo the routine resection of the right-sided colon, including the ileocecal valve. This is a randomized controlled study. Patients enrolled will be randomly assigned to the experimental group (ileocecal valve reconstruction during surgery) or the control group (no ileocecal valve reconstruction), with no differences in other treatment procedures. After a series of follow-up observations, the research team will analyze the safety and effectiveness of the method of ileocecal valve reconstruction.

Interventions

PROCEDURERISE (Revolute Insert Side-End ileocecal valve reconstruction)

After performing a conventional right hemicolectomy, an additional step is carried out in which sutures are used to artificially reconstruct an ileocecal valve structure at the ileal stump before proceeding with the ileocolic anastomosis.

Sponsors

Army Medical University, China
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Subjects aged 18-80 years; * ASA score ≤ 3; * Patients newly diagnosed with tumors located in the appendix, ileocecal region, ascending colon, hepatic flexure of the colon, or the right one-third of the transverse colon, or those scheduled to undergo laparoscopic radical right hemicolectomy; * No history of other gastrointestinal diseases (except for intestinal polyps or gallstones); * Willing to participate in the study and sign the informed consent form; * Complete clinical data available.

Exclusion criteria

* Presence of other malignant tumors in different organs; * Tumor invasion into adjacent organs; * Patients with concurrent infectious diseases or autoimmune diseases (e.g., Crohn's disease); * Patients with congenital or acquired metabolic disorders; * Use of antibiotics or other microbiota-altering medications within one month prior to enrollment; * Changes in surgical plan resulting in the resection not including the ileocecal valve.

Design outcomes

Primary

MeasureTime frameDescription
Time to first formed stool after surgery (Bristol stool score < 4).1 week after surgeryAccording to the Bristol stool scale, stools are categorized into seven types. Since stool form is related to the duration of colonic transit, the scale can be used to assess intestinal transit time and evaluate anastomotic function. A score \>5 is defined as diarrhea, with a score of 6 indicating mild diarrhea and a score of 7 indicating severe diarrhea.

Secondary

MeasureTime frameDescription
anastomosis timeduring surgery
intraoperative blood lossduring surgery
Complications within 30 days after surgery30 days after surgerySurgical complications evaluation was based on the Clavien-Dindo complication scoring system. Grade I Any deviation from the normal postoperative course without the need for pharmacological treatment or surgical, endoscopic and radiological interventions Allowed therapeutic regimens are: drugs as antiemetics, antipyretics, analgetics, diuretics and electrolytes and physiotherapy. This grade also includes wound infections opened at the bedside. Grade II Requiring pharmacological treatment with drugs other than such allowed for grade I complications. Blood transfusionsand total parenteral nutritionare also included. Grade III Requiring surgical, endoscopic or radiological intervention Grade IV Life-threatening complication (including CNS complications)\* requiring IC/ICU-management Grade V Death of a patient
anastomosis healing3 months, 6 months and 1 year after surgeryColonoscopy is used to assess the healing status of an anastomosis, and to determine whether stenosis, ulcers, or other pathological changes have occurred.
albumin level3 days, 1 month, 3 months, 6 months and 1 year after surgery.for assessing the nutritional status.
Operation timeduring the surgery
VitB123 days, 1 month, 3 months, 6 months and 1 year after surgeryfor assessing the nutritional status.
total protein3 days, 1 month, 3 months, 6 months and 1 year after surgeryfor assessing the nutritional status
EORTCQLQ-C30baseline, 1 month after surgery.for assessing quality of life after surgery
EORTCQLQ-CR2930baseline, 1 month after surgery.for assessing quality of life after surgery
gut microbiota1 month, 3 months, 6 months and 1 year after surgery.Analyzing the changes in gut microbiota through the patient's fecal samples.
bile acid3 days, 1 month, 3 months, 6 months and 1 year after surgeryfor assessing the nutritional status.

Contacts

Primary ContactWeidong Xiao, MD
xiaoweidong@tmmu.edu.cn86-13996390860
Backup ContactZihan Wang, Ph.D
shakehanhanhan@hotmail.com86-13618347369

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026