search
Back to results

Impact of Hybrid-ESD+ and LiftUp® on the en Bloc/R0 Rate in Colorectal Adenomas Between 2 and 3 cm (HADRIAN)

Primary Purpose

Colorectal Adenoma

Status
Withdrawn
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Hybrid ESD+
Sponsored by
Wuerzburg University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Colorectal Adenoma focused on measuring Hybrid-ESD+, Endoscopic Resection

Eligibility Criteria

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

Inclusion Criteria:

  • Non-pedunculated lesion in the colorectum (epithelial lesion, 2-3 cm).
  • Ablation medically indicated and possible (coagulation, etc. - as determined by the center)

Exclusion Criteria:

  • Age < 18 years
  • Pedunculated lesion (Paris0-Ip)
  • Size of the lesion <2cm or >3cm
  • Pregnant and breastfeeding women
  • Patient not capable of informed consent / consent not possible
  • Bioptic evidence of a carcinoma / high probability of the presence of a carcinoma
  • Non-lifting sign / known recurrence after previous therapy
  • Impassable stenosis in the colon / rectum
  • Patients with compelling need for therapeutic anticoagulation or dual antiplatelet therapy that cannot be discontinued for resection
  • As per contraindications from the AWC & LiftUp Instructions for Use:
  • The AWC is not to be used if flexible-endoscopic procedures are contraindicated.
  • The LiftUp gel should not be used when flexible endoscopic procedures are contraindicated, especially in combination with submucosal endoscopic resection (EMR) or endoscopic submucosal dissection (ESD) injectables.
  • LiftUp gel should not be used in patients with known sensitivity to any of the ingredients.

Sites / Locations

  • Mathilden Hospital Herford
  • Agaplesion Diakonie Kliniken Kassel
  • Klinikum Ludwigsburg
  • St. Franziskus Hospital Münster
  • Universitätsklinikum Ulm
  • Rems-Murr-Klinikum Winnenden
  • Universitätsklinik Würzburg
  • Inselspital Bern
  • Stadtspital Waid

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Hybrid-ESD+

Arm Description

All participants receive resection of non-pedunculated colorectal polyp between 2 and 3 cm using the Hybrid-ESD+ method.

Outcomes

Primary Outcome Measures

R0 resection rate of non pedunculated colorectal polyps between 2 and 3cm using hybrid ESD+
In how many cases a complete R0 resection (basal and lateral margin) is found on pathologic examination

Secondary Outcome Measures

Complication rate (perforations, bleeding)
Perforation: dehiscence of the muscularis propria diagnosed during or after resection. Hemorrhage: Clinically significant post-endoscopic bleeding (CSPEB). Bleeding from the ablation site with hematochezia after completion of index colonoscopy Intraprocedural bleeding (IPB). Percent, defined as bleeding lasting > 60 seconds during intervention necessitating therapy
Recurrence rate
Rate of adenoma residue and/or adenoma recurrence in percent after 6 months. This is determined by the colonoscopic and histologic findings from 2 biopsies from the scar or resection specimen.
Procedural parameters - Intervention duration
Intervention duration (time range from injection to complete resection)
Procedural parameters - Cleanliness of the colon
Cleanliness of the colon (according to the Boston Bowel Preparation Scale (BBPS) 0-9)
Localization of polyp
Position of the polyp within the colon (Coecum, Ascendens, Transversum, Deschendens, Sigmoid, Rectum)
Polyp size
Polyp diameter in mm
Polyp morphology
according to paris classification
Polyp histology
histological examination (tubular, tubulovillous, villous)
Duration of hospital stay
Time frame from first day to discharge

Full Information

First Posted
August 12, 2022
Last Updated
August 17, 2023
Sponsor
Wuerzburg University Hospital
Collaborators
Waid City Hospital, Zurich, University Hospital Ulm, Rems-Murr-Klinikum Winnenden, Insel Gruppe AG, University Hospital Bern, Klinikum Ludwigsburg, Mathilden Hospital Herford, St. Franziskus Hospital Münster, Agaplesion Kliniken Kassel, Ovesco Endoscopy AG
search

1. Study Identification

Unique Protocol Identification Number
NCT05517369
Brief Title
Impact of Hybrid-ESD+ and LiftUp® on the en Bloc/R0 Rate in Colorectal Adenomas Between 2 and 3 cm
Acronym
HADRIAN
Official Title
Impact of Using Hybrid-ESD+ and LiftUp® as Injectable on en Bloc/R0 Rate in Colorectal Adenomas Between 2 and 3 cm.
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Withdrawn
Why Stopped
No participants fitting into the study
Study Start Date
March 1, 2023 (Actual)
Primary Completion Date
April 2024 (Anticipated)
Study Completion Date
October 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Wuerzburg University Hospital
Collaborators
Waid City Hospital, Zurich, University Hospital Ulm, Rems-Murr-Klinikum Winnenden, Insel Gruppe AG, University Hospital Bern, Klinikum Ludwigsburg, Mathilden Hospital Herford, St. Franziskus Hospital Münster, Agaplesion Kliniken Kassel, Ovesco Endoscopy AG

4. Oversight

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

5. Study Description

Brief Summary
This study examines whether the use of Hybrid-ESD+ with LiftUp (Injection solution) results in a higher en bloc and/or R0 rate for non pedunculated colorectal adenomas between 2 and 3 cm than described in the literature for conventional EMR.
Detailed Description
There are several options for endoscopic polypectomy of polyps between 2-3 cm, all of which have their advantages and disadvantages and none of which has yet become the established standard procedure. Conventional EMR has the disadvantage of more frequent residuals and/or recurrences due to lack of en bloc resection, while ESD has the disadvantage of being more complex and complications more likely. A possible alternative is the use of hybrid ESD+ with LiftUp subcutaneous injection. The method with the LiftUp gel forming a stable gel cushion under the lesion, in combination with the circular circumcision of the mucosa at this site and the AWC for the current loop and the grasper, could achieve a better en bloc resection rate with a low complication rate than other procedures mentioned above. The higher effectiveness in terms of recurrences and complications could subsequently result in a reduction of endoscopic or surgical re-interventions. In this study, non-pedunculated colorectal polyps between 2 and 3cm in size are resected using ESD+ method and lift up as an injection solution. Methodological and clinical parameters are recorded. After 4 weeks, the patients are contacted by telephone to record possible late effects. If an endoscopic control is performed after 6 months (according to the guideline or according to the investigator), the findings are also recorded.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Adenoma
Keywords
Hybrid-ESD+, Endoscopic Resection

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Hybrid-ESD+
Arm Type
Experimental
Arm Description
All participants receive resection of non-pedunculated colorectal polyp between 2 and 3 cm using the Hybrid-ESD+ method.
Intervention Type
Procedure
Intervention Name(s)
Hybrid ESD+
Intervention Description
Injection of the Lift Up solution, followed by circumcision of the lesion using a snare tip or ESD knife. Using an additional working channel (AWC), the lesion is resected using a grasper and snare.
Primary Outcome Measure Information:
Title
R0 resection rate of non pedunculated colorectal polyps between 2 and 3cm using hybrid ESD+
Description
In how many cases a complete R0 resection (basal and lateral margin) is found on pathologic examination
Time Frame
after 14 days
Secondary Outcome Measure Information:
Title
Complication rate (perforations, bleeding)
Description
Perforation: dehiscence of the muscularis propria diagnosed during or after resection. Hemorrhage: Clinically significant post-endoscopic bleeding (CSPEB). Bleeding from the ablation site with hematochezia after completion of index colonoscopy Intraprocedural bleeding (IPB). Percent, defined as bleeding lasting > 60 seconds during intervention necessitating therapy
Time Frame
up to 4 weeks
Title
Recurrence rate
Description
Rate of adenoma residue and/or adenoma recurrence in percent after 6 months. This is determined by the colonoscopic and histologic findings from 2 biopsies from the scar or resection specimen.
Time Frame
6 months
Title
Procedural parameters - Intervention duration
Description
Intervention duration (time range from injection to complete resection)
Time Frame
1 day
Title
Procedural parameters - Cleanliness of the colon
Description
Cleanliness of the colon (according to the Boston Bowel Preparation Scale (BBPS) 0-9)
Time Frame
1 day
Title
Localization of polyp
Description
Position of the polyp within the colon (Coecum, Ascendens, Transversum, Deschendens, Sigmoid, Rectum)
Time Frame
1 day
Title
Polyp size
Description
Polyp diameter in mm
Time Frame
1 day
Title
Polyp morphology
Description
according to paris classification
Time Frame
1 day
Title
Polyp histology
Description
histological examination (tubular, tubulovillous, villous)
Time Frame
7 days
Title
Duration of hospital stay
Description
Time frame from first day to discharge
Time Frame
up to 4 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Non-pedunculated lesion in the colorectum (epithelial lesion, 2-3 cm). Ablation medically indicated and possible (coagulation, etc. - as determined by the center) Exclusion Criteria: Age < 18 years Pedunculated lesion (Paris0-Ip) Size of the lesion <2cm or >3cm Pregnant and breastfeeding women Patient not capable of informed consent / consent not possible Bioptic evidence of a carcinoma / high probability of the presence of a carcinoma Non-lifting sign / known recurrence after previous therapy Impassable stenosis in the colon / rectum Patients with compelling need for therapeutic anticoagulation or dual antiplatelet therapy that cannot be discontinued for resection As per contraindications from the AWC & LiftUp Instructions for Use: The AWC is not to be used if flexible-endoscopic procedures are contraindicated. The LiftUp gel should not be used when flexible endoscopic procedures are contraindicated, especially in combination with submucosal endoscopic resection (EMR) or endoscopic submucosal dissection (ESD) injectables. LiftUp gel should not be used in patients with known sensitivity to any of the ingredients.
Facility Information:
Facility Name
Mathilden Hospital Herford
City
Herford
ZIP/Postal Code
32052
Country
Germany
Facility Name
Agaplesion Diakonie Kliniken Kassel
City
Kassel
ZIP/Postal Code
34119
Country
Germany
Facility Name
Klinikum Ludwigsburg
City
Ludwigsburg
ZIP/Postal Code
71640
Country
Germany
Facility Name
St. Franziskus Hospital Münster
City
Münster
ZIP/Postal Code
48145
Country
Germany
Facility Name
Universitätsklinikum Ulm
City
Ulm
ZIP/Postal Code
89081
Country
Germany
Facility Name
Rems-Murr-Klinikum Winnenden
City
Winnenden
ZIP/Postal Code
71364
Country
Germany
Facility Name
Universitätsklinik Würzburg
City
Würzburg
ZIP/Postal Code
97080
Country
Germany
Facility Name
Inselspital Bern
City
Bern
ZIP/Postal Code
3010
Country
Switzerland
Facility Name
Stadtspital Waid
City
Zürich
ZIP/Postal Code
8037
Country
Switzerland

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Impact of Hybrid-ESD+ and LiftUp® on the en Bloc/R0 Rate in Colorectal Adenomas Between 2 and 3 cm

We'll reach out to this number within 24 hrs