Efficacy and Safety of Robot-assisted Endoscopic Submucosal Dissection for Colorectal Neoplasm

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-85
SponsorShandong University

About this trial

The objective of this study is to investigate the role of the flexible auxiliary single-arm transluminal endoscopic robot (FASTER) system in colorectal endoscopic submucosal dissection (ESD) and to validate its superiority over conventional ESD in terms of reducing procedural difficulty, shortening procedure time, and enhancing procedural safety.

The main questions it aims to answer are:

Does the use of the FASTER system improve the dissection speed of the ESD procedure? Does the use of the FASTER system reduce the procedure and dissection time, improving the efficacy of the ESD procedure? Does the use of the FASTER system reduce the rate of perforation and hemorrhage, improving the safety of the ESD procedure? Researchers will compare FASTER-assisted ESD and conventional ESD to evaluate the safety and efficacy of the FASTER system.

Participants will:

Be randomly assigned to the group with ESD using the traditional procedure or to the group with ESD assisted by the FASTER system.

Keep a diary of their symptoms after the procedure. ESD has gained widespread acceptance as the standard method for treating early-stage gastrointestinal cancers. However, ESD is a technically demanding and intricate procedure that requires advanced proficiency of operators, with a heightened risk of complications such as hemorrhage and perforation. The inherent challenges of the colorectal ESD are further amplified by the thin mucosa, highly tortuous and flexible lumen, and occasional obstruction of lesions by mucosal folds, all of which collectively elevate both the procedural difficulty and the probability of postoperative complications. Adequate exposure of the submucosa layer through effective tissue traction is vital for the safe and effective performance of ESD. The FASTER system is designed to overcome this technical difficulty.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients aged 18-85.

Patients with pathologically verified colorectal neoplasms scheduled to undergo ESD.

Disqualifiers

Patients have lesions with confirmed or potential deep submucosal invasion or lymph node metastasis or other conditions that are not suitable for endoscopic therapy.

Patients with severe underlying diseases precluding endotracheal intubation, general anesthesia, or surgery.

Patients have a history of colorectal malignancy with previous radiotherapy or operative treatment leading to changes in colorectal structure.

Patients have lesions with local recurrence after endoscopic resection.

Trial design

Design model

Parallel

Treatments tested in this trial

  • FASTER-assisted ESD

    Procedure/Surgery

    The patients who are randomly assigned to the FASTER-assisted ESD group will undergo the ESD procedure with the assistance of the FASTER system.

  • Conventional ESD

    Procedure/Surgery

    The patients who are randomly assigned to the conventional ESD group will undergo the ESD following the clinically established pattern.

Treatment groups

104 Participants
are divided into 2 treatment groups
Group A: FASTER-assisted ESDExperimental treatment 1 intervention
Group B: Conventional ESDActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

procedure time

Procedure time is the time from the beginning of injection to the completion of dissection.

Time frame
Within 24 hours after the procedure.

Secondary outcomes

1

dissection time

Dissection time is the time from the beginning of dissection to the completion of dissection.

Time frame
Within 24 hours after the procedure.
2

dissection speed

Dissection speed is defined as the lesion area divided by the dissection time.

Time frame
Within 24 hours after the procedure.
3

en bloc resection rate

En bloc dissection refers to the complete removal of the entire lesion in a single piece.

Time frame
Within 24 hours after the procedure.
4

R0 resection rate

R0 resection is defined as en bloc resection with negative vertical and horizontal margins.

Time frame
Within 24 hours after the procedure.

Other outcomes

Sponsors and contacts

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