Laparoscopy Clinical Trial
— IVEAOfficial title:
Intracorporeal Vs Extracorporeal Anastomosis in Patients Undergoing Laparoscopic Right Hemicolectomy: a Multicenter Randomized Clinical Trial (The IVEA-study)
Verified date | June 2019 |
Source | Hospital Universitario Torrecárdenas |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Objective. The aim of this study was to evaluate short-term outcomes of performing
intracorporeal versus extracorporeal anastomosis in laparoscopic right hemicolectomy for
right colon neoplasm. Background. Despite advances in laparoscopic approach in colorectal
surgery and the clear benefit of this approach over open surgery, the technical difficulty in
performing intracorporeal anastomosis causes certain groups continue performing it
extracorporeally in right colon surgery.
Methods. This study was a prospective multicenter randomized trial with two parallel groups
being done intracorporeal anastomosis (IA) or extracorporeal anastomosis (EA) in laparoscopic
right hemicolectomy for right colon neoplasm, carried out between January 2016 and December
2018.
Status | Completed |
Enrollment | 168 |
Est. completion date | December 31, 2018 |
Est. primary completion date | December 31, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - All patients had to be 18 years of age or over, to be programmed for laparoscopic surgery for right colon neoplasm and provide a signed written consent form. Exclusion Criteria: - All patients who do not meet all the inclusion criteria were excluded. The other exclusion criteria included the need for emergency surgery, renal failure defined by haemodialysis, Crohn's disease, ulcerative colitis, T4 tumor invading adjacent organs, synchronous colorectal neoplasm, metastasis or carcinomatosis at diagnosis, bowel obstruction, psychiatric disorders or contraindication for laparoscopic approach. |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Hospital Universitario Torrecárdenas | Sponsor- Investigator MD Ángel Reina Duarte. HUTorrecárdenas, Sponsor-Investigator BA Francisco Rubio Gil. HU Torrecárdenas, Sponsor-Investigator MD Almudena Moreno Serrano. Hospital Inmaculada. Huercal-Overa, Sponsor-Investigator MD Elisabet Vidaña Márquez. HU Torrecárdenas, Sponsor-Investigator MD Jorge Alejandro Benavides Buleje. HU Reina Sofía, Sponsor-Investigator MD Juan Manuel García Torrecillas. HU Torrecárdenas, Sponsor-Investigator MD Pedro Moya Forcén. HU Torrecárdenas, Sponsor-Investigator Rocío Torres Fernández. HU Torrecárdenas |
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* Note: There are 20 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | In patients with right colon cancer, laparoscopic right hemicolectomy with intracorporeal anastomosis presents less perioperative morbidity than extracorporeal anastomosis. | To compare perioperative morbidity between laparoscopic right hemicolectomy with intracorporeal anastomosis versus extracorporeal anastomosis within 30 days after surgery. | 24 months | |
Secondary | Surgical time | o evaluate the difference in surgical time between right hemicolectomy with intracorporeal versus extracorporeal anastomosis. | 4 hours | |
Secondary | VAS | Quantify, by means of the Visual-Analogue Scale (VAS: is determined by measuring the distance (mm) on the 10-cm line between the "no pain" anchor and the patient's mark, providing a range of scores from 0-100. A higher score indicates greater pain intensity. Based on the distribution of pain VAS scores in post- surgical patients who described their postoperative pain intensity as none, mild, moderate, or severe, the following cut points on the pain VAS have been recommended: no pain (0-4 mm), mild pain(5-44 mm), moderate pain (45-74 mm), and severe pain (75-100 mm)), postoperative pain 24 hours after surgery and the day of hospital discharge, and determine which of the two laparoscopic right hemicolectomy techniques produces less pain. | 24 hour | |
Secondary | Dehiscence | To evaluate and compare the rate of anastomotic dehiscence in both groups of anastomoses up to 30 days after surgery. | 30 days | |
Secondary | Infection rate | To evaluate the infection rate of the surgical site in both groups up to 30 days after surgery. | 30 days | |
Secondary | Days of hospital stay | o compare the difference of days of hospital stay in both groups of anastomoses. | 180 days |
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