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Trial for Retractor Sponge Evaluation in Laparoscopic Colorectal Surgery (SPONGE)

Primary Purpose

Colon Carcinoma, Rectum Carcinoma

Status
Unknown status
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Sponge
Sponsored by
St. Antonius Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Colon Carcinoma focused on measuring Laparoscopic colorectal surgery, Retractor sponge, Trendelenburg position, Postoperative complications

Eligibility Criteria

18 Years - 95 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria:

  • Participant in the PICNIC project (METC 12-510)
  • Informed consent obtained for being offered experimental interventions within the PICNIC project
  • Informed consent obtained for questionnaires on patient reported outcomes within the PICNIC project
  • Planned for laparoscopic surgery of distal colorectal cancer in St. Antonius Hospital

Exclusion Criteria:

  • Planned for open colorectal surgery
  • Surgery for benign colorectal diseases
  • Emergency colorectal surgery
  • Inadequate understanding of the Dutch language in speech and/or writing

Sites / Locations

  • St. Antonius HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Sponge group

Control group

Arm Description

Patients offered surgery with the retractor sponge

Patients receiving standard care: surgery in Trendelenburg position

Outcomes

Primary Outcome Measures

Postoperative hospital stay (days)
Based on a discharge checklist

Secondary Outcome Measures

Operation time
minutes
Blood-loss peroperative
ml
Diuretics peroperative and postoperative
mg
Postoperative hypoxemia
O2 saturation
Peri- and postoperative surgical complications
number
Pulmonary complications.
number
Cardiac complications
number

Full Information

First Posted
May 4, 2017
Last Updated
May 29, 2019
Sponsor
St. Antonius Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03334383
Brief Title
Trial for Retractor Sponge Evaluation in Laparoscopic Colorectal Surgery
Acronym
SPONGE
Official Title
Randomized Controlled Trial to Evaluate the Effect of a Retractor Sponge in Postoperative Hospital Stay in Laparoscopic Colorectal Surgery in Patients With Malignancy
Study Type
Interventional

2. Study Status

Record Verification Date
May 2019
Overall Recruitment Status
Unknown status
Study Start Date
January 2015 (Actual)
Primary Completion Date
June 2020 (Anticipated)
Study Completion Date
October 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
St. Antonius Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Laparoscopic surgery of the distal colon and rectum requires surgery with an appropriate field of view. A commonly used technique to create a clear exposure is the steep Trendelenburg position in which the patient is positioned in an angle of 15 to 40 degrees with the head down using the effect of gravity to retract the small intestine. This method is associated with haemostatic changes caused by the cranial shift of abdominal organs and blood. Recently, a cellulose compressed sponge was developed as intraoperative retractor, with the aim to keep the small intestines aside while the patient remains in a horizontal position. The safety of the sponge is secured with CE marking. The retractor sponge ensures a clear surgical field and potentially prevents haemostatic instability by avoiding Trendelenburg position. A pilot study in the St Antonius Hospital Nieuwegein has shown that use of the sponge might be associated with shorter hospital stay.
Detailed Description
Objective: We study the efficacy of the retractor sponge in laparoscopic colorectal surgery to reduce hospital stay in patients operated for a malignancy. Secondary objectives are duration of surgery, blood-loss, use of diuretics as volume therapy (during surgery as wells as during total hospital stay), postoperative hypoxemia and peri- and postoperative complications. Study design: Randomized controlled trial, nested within a prospective cohort according to the 'cohort multiple randomized controlled trial' (cmRCT) design. Study population: Patients with colorectal cancer who undergo laparoscopic surgery, and who have given informed consent to be offered experimental interventions within the PICNIC project. Patient who require open surgery or patients with benign colorectal diseases are excluded for this study. Intervention: Intraoperative use of the retractor sponge versus usual care, i.e. the Trendelenburg position. Main study parameters/endpoints: The primary endpoint is length of hospital stay. Secondary endpoints are duration of surgery, blood-loss, use of diuretics (during surgery as wells as during total hospital stay), postoperative hypoxemia and peri- and postoperative surgical, pulmonary and cardiac complications. Nature and extent of the burden and risks associated with participation, benefit and group relatedness: The study will be conducted according to the cohort multiple Randomized Controlled Trial (cmRCT) design. Within the PICNIC cohort, we will identify all patients who are eligible for the experimental intervention (use of the sponge) and who have given informed consent to be invited for future experimental interventions. From this sub cohort, we will randomly select a group of patients to whom we will offer surgery with use of the retractor sponge, which they can accept or decline. Eligible patients from the sub cohort who were not randomly selected will undergo standard treatment, i.e. surgery in Trendelenburg position. We do not expect adverse events in patients in the intervention arm, besides dysfunction of the sponge, after which conversion to standard treatment (Trendelenburg position) needs to take place.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colon Carcinoma, Rectum Carcinoma
Keywords
Laparoscopic colorectal surgery, Retractor sponge, Trendelenburg position, Postoperative complications

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Sponge group
Arm Type
Experimental
Arm Description
Patients offered surgery with the retractor sponge
Arm Title
Control group
Arm Type
No Intervention
Arm Description
Patients receiving standard care: surgery in Trendelenburg position
Intervention Type
Device
Intervention Name(s)
Sponge
Other Intervention Name(s)
Endoractor, Kawamoto corporation (Osaka, Japan)
Intervention Description
Compressed cellulose sponge for use in laparoscopic surgery to retract the intestines from the surgical field.
Primary Outcome Measure Information:
Title
Postoperative hospital stay (days)
Description
Based on a discharge checklist
Time Frame
Up to 4 weeks
Secondary Outcome Measure Information:
Title
Operation time
Description
minutes
Time Frame
Up to 4 hours
Title
Blood-loss peroperative
Description
ml
Time Frame
During surgery time
Title
Diuretics peroperative and postoperative
Description
mg
Time Frame
Up to 4 weeks (during hospital stay)
Title
Postoperative hypoxemia
Description
O2 saturation
Time Frame
Up to 1 week
Title
Peri- and postoperative surgical complications
Description
number
Time Frame
Up to 4 weeks
Title
Pulmonary complications.
Description
number
Time Frame
Up to 4 weeks
Title
Cardiac complications
Description
number
Time Frame
Up to 4 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
95 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria: Participant in the PICNIC project (METC 12-510) Informed consent obtained for being offered experimental interventions within the PICNIC project Informed consent obtained for questionnaires on patient reported outcomes within the PICNIC project Planned for laparoscopic surgery of distal colorectal cancer in St. Antonius Hospital Exclusion Criteria: Planned for open colorectal surgery Surgery for benign colorectal diseases Emergency colorectal surgery Inadequate understanding of the Dutch language in speech and/or writing
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Anke B Smits, MD
Phone
0031883201919
Email
absmits@antoniusziekenhuis.nl
First Name & Middle Initial & Last Name or Official Title & Degree
Alice M Couwenberg, BSc
Phone
0031640904560
Email
alice.couwenberg@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anke B Smits, MD
Organizational Affiliation
St. Antonius Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
St. Antonius Hospital
City
Nieuwegein
State/Province
Utrecht
ZIP/Postal Code
3430EM
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Anke B Smits, MD
Phone
088 3201919
Email
absmits@antoniusziekenhuis.nl
First Name & Middle Initial & Last Name & Degree
Alice M Couwenberg, BSc
Phone
0031640904560
Email
alice.couwenberg@gmail.com
First Name & Middle Initial & Last Name & Degree
Anke B Smits, MD/PhD
First Name & Middle Initial & Last Name & Degree
Alice M Couwenberg, BSc
First Name & Middle Initial & Last Name & Degree
Johannes PM Burbach, MD
First Name & Middle Initial & Last Name & Degree
Helena M Verkooijen, MD/AssProf
First Name & Middle Initial & Last Name & Degree
Peter G Noordzij, MD/PhD
First Name & Middle Initial & Last Name & Degree
Onne Reerink, MD/PhD
First Name & Middle Initial & Last Name & Degree
Marco van Vulpen, MD/Prof

12. IPD Sharing Statement

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Trial for Retractor Sponge Evaluation in Laparoscopic Colorectal Surgery

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