RECSINSMTs: A Randomized Controlled Clinical Study on the Application of the Third Space in the Operation of Gastric Submucosal Tumor

Sponsor
First Affiliated Hospital Xi'an Jiaotong University (Other)
Overall Status
Unknown status
CT.gov ID
NCT03612830
Collaborator
Air Force Military Medical University, China (Other)
80
1
2
32.7
2.4

Study Details

Study Description

Brief Summary

Gastric submucosal tumors (SMTs) are rare findings during routine upper endoscopy; the incidence of these lesions may be as high as 0.4%.SMTs display a wide spectrum,ranging from benign to highly malignant, with gastrointestinal stromal tumors (GISTs) being the most common type.SMTs is a gastrointestinal tumor,surgical operation is still the main method of gastric tumor treatment.The common surgical methods for resection of SMTs include laparotomy and laparoscopic surgery.In recent years, the Da Vinci robot assisted gastric resection has become a new way to treat gastric cancer. Compared with the traditional laparoscopy and laparotomy, the operation of the robot is more precise and flexible, with obvious advantages of minimally invasive and good application value and prospect.In recent years, some scholars have put forward the concept of the third space.The concept of the "third space" was initiatively proposed at the same time when new endoscopic surgery approach via natural orifice transluminal was put forward(NOTES). To be specific, with respect to the first space(lumen) and second space(peritoneal cavity),the third space refers to the intramural space.The aim of the study is to compare value (outcomes/costs) of surgery in patients with SMTs by 2 approaches:Laparoscopic and Endoscopic cooperative surgery(LECS),Robotic and Endoscopic cooperative surgery(RECS).First of all, the investigators will collect 80 cases of SMTs patients, randomly assigned for the LECS and RECS groups. Secondly, to analyzing the demographic data,basic treatment and follow-up data, including the operation time, blood loss, the number of cut edge positive, the distances of cut edge away from the tumor edge, average such confinement, the meal time, cost of treatment, tumor recurrence rate, the presence of residual stomach, upset stomach and frequency,complications and other indicators.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Laparoscopy endoscopy cooperated surgery
  • Procedure: Dan Vinchi robot endoscopy cooperated surgery
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
80 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Laparoscopic and Endoscopic cooperative sugery,Robotic and Endoscopic cooperative sugeryLaparoscopic and Endoscopic cooperative sugery,Robotic and Endoscopic cooperative sugery
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Comparison of Laparoscopic and Endoscopic Cooperative Surgery and Robotic and Endoscopic Cooperative Surgery in the Operation of Gastric Submucosal Tumor
Actual Study Start Date :
Apr 11, 2018
Anticipated Primary Completion Date :
Jun 30, 2020
Anticipated Study Completion Date :
Dec 30, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: LECS

Laparoscopic and Endoscopic cooperative surgery,LECS resects the tumor completely by laparoscopy with the help of the precise positioning and guidance of endoscopy .

Procedure: Laparoscopy endoscopy cooperated surgery
LECS resects the tumor completely by laparoscopy with the help of the precise positioning and guidance of endoscopy

Experimental: RECS

Robotic and Endoscopic cooperative surgery,RECS resects the tumor completely by Dan Vinchi robot with the help of the precise positioning and guidance of endoscopy .

Procedure: Dan Vinchi robot endoscopy cooperated surgery
RECS resects the tumor completely by Dan Vinchi Robot with the help of the precise positioning and guidance of endoscopy

Outcome Measures

Primary Outcome Measures

  1. operation time [1 hours to 6 hours through the surgery completion]

    record in minutes,from the beginning of anesthesia to the end

Secondary Outcome Measures

  1. blood loss [1 hours to 6 hours through the surgery completion]

    from the surgical record sheet

  2. success rate [from two days to two weeks after surgery]

    to ensure the integrity of the tumor and obtain the negative surgical margin

  3. time in bed [from two days to two weeks after surgery]

    the time in bed to the postoperative patient

  4. time to take food [from two days to two weeks after surgery]

    the time to eat to the postoperative patient

  5. postoperative complication rate [from two weeks to one year after surgery]

    including anastomotic stoma fistula,anastomotic stenosis,abdominal infection,postoperative bleeding

  6. tumor recurrence rate [from one month to 2 years after surgery]

    periodic review the CT or MRI or endoscope

  7. hospitalization expenses [1 month]

    total hospitalization expenses

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients without contraindications gastroscope,surgery and anesthesia;

  • Gastroscope found submucosal lesions, qualitative hard;Endoscopic ultrasonography (EUS) confirmed the lesions come from the muscularis propria;

  • Tumors diameter > 2 cm;Or tumors had < 2 cm, but the position is located in the stomach wall, after nearly cardia and it is a difficult position for gastroscope ;

  • Tumors diameter < 5 cm, the tumors had complete, no broken feed and bleeding;

  • Not found the tumor metastasis;

  • There is no history of abdominal surgery, no severe abdominal cavity adhesion

  • Normal coagulation function;

  • There is no history of anticoagulant drugs, or who take aspirin, salvia miltiorrhiza, etc., should stop taking drugs for more than one week;

  • Patients and their families volunteered choice the surgical procedure and signed informed consent.

Exclusion Criteria:
  • Patients with preoperative assessment of distant metastasis;

  • Patients with preoperative radiation and chemotherapy or hormone therapy;

  • Patients with acute obstruction, bleeding or perforation of the emergency surgery;

  • Patients with a history of abdominal trauma or abdominal surgery;

  • Patients with contraindications gastroscope,surgery and anesthesia.

Contacts and Locations

Locations

Site City State Country Postal Code
1 First Affiliated Hospital of Xi'an Jiaotong University Xi'an Shaanxi China 710061

Sponsors and Collaborators

  • First Affiliated Hospital Xi'an Jiaotong University
  • Air Force Military Medical University, China

Investigators

  • Principal Investigator: Jun Jun She, First Affiliated Hospital Xi'an Jiaotong University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
First Affiliated Hospital Xi'an Jiaotong University
ClinicalTrials.gov Identifier:
NCT03612830
Other Study ID Numbers:
  • XJYFY-2018W411
First Posted:
Aug 2, 2018
Last Update Posted:
Aug 15, 2018
Last Verified:
Apr 1, 2018
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by First Affiliated Hospital Xi'an Jiaotong University

Study Results

No Results Posted as of Aug 15, 2018