search
Back to results

Perianastomotic Drain After Gastrectomy (DRAG) (DRAG)

Primary Purpose

Gastric Cancer

Status
Recruiting
Phase
Not Applicable
Locations
Greece
Study Type
Interventional
Intervention
No drain placement
Sponsored by
THEODOROU DIMITRIOS
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Gastric Cancer focused on measuring perianastomotic drain, gastrectomy, complication detection

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age more than or equal to 18 years
  • Histologically proven gastric or gastro-esophageal cancer
  • Patients that undergo open total D2 gastrectomy with Roux-en-Y reconstruction
  • ECOG (Eastern Cooperative Oncology Group) performance status 0 or 1
  • Curative resection
  • Signed informed consent form

Exclusion Criteria:

  • Metastatic disease
  • Additional resections needed
  • Ascites
  • Cachexia
  • Concurrent participation in other study(ies)
  • Concurrent diagnosis of mental illness
  • Lack of perioperative protocol compliance
  • Pregnancy

Sites / Locations

  • Hippocration General HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Drain

No drain

Arm Description

The patients of this arm undergo perianastomotic drain placement, as per standard of care institutional practice

The patients of this arm do not undergo perianastomotic drain placement.

Outcomes

Primary Outcome Measures

POD of intra-abdominal complication detection
Post-operative day of class II-IV intra-abdominal complication detection

Secondary Outcome Measures

Hospital stay
Hospital stay (in days)
Mortality
Mortality
Morbidity
Total Morbidity
Drain related morbidity
Drain related morbidity
Post-operative pain: visual analogue scale (VAS) score
Post-operative pain assessment with visual analogue scale (VAS) score
Quality of life before and after gastrectomy: questionnaire assessment
Quality of life questionnaire assessment
Readmissions
Readmission rate

Full Information

First Posted
February 23, 2020
Last Updated
March 29, 2022
Sponsor
THEODOROU DIMITRIOS
search

1. Study Identification

Unique Protocol Identification Number
NCT04288661
Brief Title
Perianastomotic Drain After Gastrectomy (DRAG)
Acronym
DRAG
Official Title
Assessment of Abdominal Perianastomotic Drain Placement After Open Gastrectomy for Gastric Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
March 2022
Overall Recruitment Status
Recruiting
Study Start Date
February 28, 2020 (Actual)
Primary Completion Date
February 2024 (Anticipated)
Study Completion Date
June 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
THEODOROU DIMITRIOS

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The placement of an abdominal drain consists one of the most controversial issues not only after gastrectomy, but also after any abdominal operation in general. During the past decades drains have been widely used after major abdominal operations. Nevertheless, following the latest perioperative management trends, not all surgeons seem to embrace the idea. There are still many new studies or in progress, mainly in the East, examining the prognostic value of the drain content after a gastrectomy. Thus, the use of a drain is still under question. The aim of the present study is to evaluate whether the placement of a perianastomotic drain after total gastrectomy with D2 lymphadenectomy contributes to the early diagnosis of intraabdominal complications such as bleeding, abscess, anastomotic leak or pancreatic fistula. The participants will be patients with pathologically confirmed gastric or gastroesophageal junction (GEJ) cancer, and will undergo total gastrectomy plus D2 lymph node dissection and Roux-en-Y gastrointestinal tract reconstruction.
Detailed Description
This is a prospective randomized controlled trial that will be conducted in the 1st Propaedeutic Department of Surgery of National and Kapodistrian University of Athens. Sixty six patients suffering from histologically confirmed gastric or gastroesophageal junction cancer will be included in the study. They will be treated with a typical total gastrectomy plus D2 lymph node dissection and Roux-en-Y gastrointestinal tract reconstruction, under a predefined perioperative protocol, which complies with the ERAS guidelines. All patients will have to sign a study specific consent form and will be educated to the perioperative protocol prior to the operation. The randomization will take place right before the abdominal wall closure, and the participants will be divided in two groups: the intervention group (without perianastomotic drain) and the control group (placement of a suction drain close to the esophagojejunal anastomosis). In the control group, the drain will be removed as usual on the fifth postoperative day only if the below criteria are satisfied: a)less than 100cc of drainage for two consecutive days and b) no clinical suspicion of anastomotic leak and/or bleeding and/or intraabdominal abscess and/or pancreatic fistula. The participants' preoperative and intraoperative data will be meticulously recorded. The postoperative course of all patients will be closely monitored and any clinical, laboratory or imaging suspicion of the above mentioned complications will be evaluated and managed as per institutional standard of care. The subjects will be followed up on postoperative days ten, thirty and sixty through clinical examination, laboratory tests and, if needed, imaging exams. The primary outcome of this trial will be the postoperative day on which a Clavien-Dindo II-IV complication will be detected. The secondary outcome measures will include length of stay, morbidity and mortality, drain- related morbidity, postoperative pain evaluation, quality of life after the operation and readmissions.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gastric Cancer
Keywords
perianastomotic drain, gastrectomy, complication detection

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
66 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Drain
Arm Type
No Intervention
Arm Description
The patients of this arm undergo perianastomotic drain placement, as per standard of care institutional practice
Arm Title
No drain
Arm Type
Experimental
Arm Description
The patients of this arm do not undergo perianastomotic drain placement.
Intervention Type
Procedure
Intervention Name(s)
No drain placement
Intervention Description
The need of perianastomotic drain placement after Roux-en-Y reconstruction in total gastrectomy operations is investigated. As intervention, no drain placement is considered
Primary Outcome Measure Information:
Title
POD of intra-abdominal complication detection
Description
Post-operative day of class II-IV intra-abdominal complication detection
Time Frame
Hospital stay, an average of 7 days
Secondary Outcome Measure Information:
Title
Hospital stay
Description
Hospital stay (in days)
Time Frame
Hospital stay, an average of 7 days
Title
Mortality
Description
Mortality
Time Frame
60 post-operative days
Title
Morbidity
Description
Total Morbidity
Time Frame
60 post-operative days
Title
Drain related morbidity
Description
Drain related morbidity
Time Frame
60 post-operative days
Title
Post-operative pain: visual analogue scale (VAS) score
Description
Post-operative pain assessment with visual analogue scale (VAS) score
Time Frame
60 post-operative days
Title
Quality of life before and after gastrectomy: questionnaire assessment
Description
Quality of life questionnaire assessment
Time Frame
60 post-operative days
Title
Readmissions
Description
Readmission rate
Time Frame
60 post-operative days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age more than or equal to 18 years Histologically proven gastric or gastro-esophageal cancer Patients that undergo open total D2 gastrectomy with Roux-en-Y reconstruction ECOG (Eastern Cooperative Oncology Group) performance status 0 or 1 Curative resection Signed informed consent form Exclusion Criteria: Metastatic disease Additional resections needed Ascites Cachexia Concurrent participation in other study(ies) Concurrent diagnosis of mental illness Lack of perioperative protocol compliance Pregnancy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Maria-Malvina Eleftheriou, MD
Phone
2132088142
Email
malvina_el@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dimitrios Theodorou, Professor
Organizational Affiliation
University of Athens
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Maria-Malvina Eleftheriou, MD
Organizational Affiliation
Hippocration General Hospital of Athens
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hippocration General Hospital
City
Athens
ZIP/Postal Code
11527
Country
Greece
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Maria- Malvina Eleftheriou, MD
Phone
2132088142
Email
malvina_el@hotmail.com

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Perianastomotic Drain After Gastrectomy (DRAG)

We'll reach out to this number within 24 hrs