Efficiency of Two Dimensional High Definition vs Three Dimensional Endoscopic Systems in Transanal Endoscopic Surgery

Corporacion Parc Tauli

Status: Completed

Conditions: Rectal Adenoma

Treatments: Procedure: Transanal endoscopic microsurgery (TEM); Procedure: 2-D high definition vision systems, transanal endoscopic operation (TEO)

Study type: Interventional

Funder types: Other

Identifiers

NCT01498354

TEO-TEM-2010-01

Details and patient eligibility

About

Introduction: The usual surgical technique for large adenomatous tumors and rectal cancer is anterior resection of the rectum or abdominoperineal resection. These techniques are associated with high mortality and morbidity and with genitourinary dysfunctions.

To solve these problems, transanal endoscopic microsurgery (TEM) was designed. Through its 3-D vision system using a rectoscope, this procedure allows access to rectal tumors located up to 20 cm from the anal verge. It is associated with minimal morbidity and has few repercussions for anal continence.

The use of 2-D high definition cameras and screens obtains images of a similar quality to 3-D images. This means that from the surgical point of view the procedure known as TEO (transanal endoscopic operation) seems as practicable as classic TEM.

Main aim: To assess the effectiveness of 2-D high definition vision systems (TEO) versus conventional 3-D (TEM) in endoscopic surgery of rectal tumors, with respect to surgical facility, postoperative morbidity, quality of the surgical specimens, and cost.

Design: Prospective, controlled, randomized study of the efficacy of the use of 2-D high definition endoscopic systems versus 3-D (TEM) in transanal endoscopic surgery.

Disease studied: Rectal adenomas and adenocarcinomas "in situ" suitable for local surgery.

Main variable evaluated: Cost per procedure assuming similar surgical efficacy and equal postoperative morbidity.

Study population and total number of patients: Patients diagnosed with rectal tumor treated with curative intent (rectal adenomas and adenocarcinomas "in situ"). The total sample calculated for the trial was 36 patients, 18 in each group (TEO and TEM).

Timing and expected finish date: After approval by the CEIC, the expected date for the inclusion of the first patient was August 2010. The study is expected to last 18-24 months.

Enrollment: 36 patients

Sex: All

Ages: 18 to 90 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients of either sex older than 18 years
• Rectal tumor identified as rectal adenoma by multifocal biopsy using colonoscopy, with endorectal ultrasound and magnetic resonance imaging findings of non-invasive tumor.
• Size of the tumor between 2 and 6 cm in maximum diameter.
• Tumor location, lower edge at least 2 cm from the anal verge, and upper edge at least 15 cm from the anal verge.
• ASA score more than III.
• intervention was performed under general anesthesia

Exclusion criteria

• Invasive adenocarcinoma shown in the final pathology study. "in situ" or intraepithelial adenocarcinomas are not excluded .
• Pregnant patients
• Patients with liver cirrhosis or blood dyscrasia.
• Patients who can not be administered under general anesthesia.
• Patients on antiplatelet or anticoagulation therapy who have not been properly prepared for surgery.
• Presence of two or more transanal endoscopic excisions in the same procedure.
• Informed consent not signed.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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36 participants in 2 patient groups

2-D high definition TEO (transanal endoscopic operation)

Experimental group

Treatment:

Procedure: 2-D high definition vision systems, transanal endoscopic operation (TEO)

Transanal endoscopic microsurgery (TEM)

Active Comparator group

Description:

Transanal endoscopic microsurgery (TEM), 3-D vision system using a rectoscope, which allows access to rectal tumors located up to 20 cm from the anal verge

Treatment:

Procedure: Transanal endoscopic microsurgery (TEM)