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The QUILT Study: Quilting Sutures in Patients Undergoing Breast Cancer Surgery (QUILT)

Primary Purpose

Seroma

Status
Not yet recruiting
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Quilting
Conventional wound closure
Sponsored by
Canisius-Wilhelmina Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Seroma focused on measuring Mastectomy, Breast cancer surgery, Quilting, Flap fixation, Seroma, Complications, Shoulder function, Pain, Cosmetic outcome, Health care consumption

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • all patients >18 years of age undergoing mastectomy and/or axillary lymph node dissection
  • be irrespective of the nature of the primary tumour: prophylactic, risk reducing, benign, in situ carcinoma and invasive primary or recurrent carcinoma will be eligible, irrespective of preoperative systemic therapy.

Exclusion Criteria:

  • patients who objected to participation (letter of objection)
  • mentally incompetent patients or otherwise unable to complete a questionnaire
  • immediate breast reconstruction
  • pregnancy

Sites / Locations

  • Canisius Wilhelmina Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Conventional closure method

Quilting

Arm Description

Following mastectomy, skin is closed using subcutaneous sutures followed by intracutaneous running suture. Depending on the surgeons discretion a vacuum closed suction drain was placed beneath the skin flaps.

The implemented intervention is the quilting suture technique. The subcutaneous tissue is sutured to the pectoralis muscle placing multiple rows of running sutures. The suture starts at either end of the scar, running back and forth, creating rows of quilting stiches. The rows are placed transversely from the cranial to the caudal end of the wound with 2-3 cm between them, totalling some three to five rows for the cranial flap. The caudal flap is quilted with 2-3 rows in a caudal to cranial fashion. A subcutaneous suture followed by a intracutaneous running suture is used to close the skin. No wound drain is placed.

Outcomes

Primary Outcome Measures

Textbook outcome
'Textbook outcome' (TO), a combination of outcome parameters reflecting an ideal surgical outcome. Measured 6 months post-operative, the patients postoperative course must comply with the following to meet the definition of TO: no wound complications no re-admissions in relation to primary surgery no re-operation in relation to primary surgery, re-excisions in case of involved margins allowed no unscheduled visit to the outpatient clinic (depending on the centre one or two postoperative visits are usually scheduled) postoperative use of analgesics (6 months) is not increased compared to pre-operative

Secondary Outcome Measures

All palpation-detected seromas
Severity of complicaties are scored using the Clavien Dindo Classification of Surgical complications (grade I-V).
Clinical significant seroma
All aspirated seroma. Severity of complicaties are scored using the Clavien Dindo Classification of Surgical complications (grade I-V).
Surgical site infections
Severity of complicaties are scored using the Clavien Dindo Classification of Surgical complications (grade I-V).
Bleeding complications
Severity of complicaties are scored using the Clavien Dindo Classification of Surgical complications (grade I-V).
Wound healing problems
Including skin flap necrosis, wound necrosis, wound dehiscence. Severity of complicaties are scored using the Clavien Dindo Classification of Surgical complications (grade I-V).
Duration of surgery
Duration of surgery in minutes.
Length of hospital stay
Length of hospital stay in days: distinguishing between outpatient and inpatient treatment.
Unscheduled visits to the outpatient clinic
Number of unscheduled visits to the outpatient clinic
Readmission to the hospital
Readmission to the hospital related to primary surgery
Reoperation
Reoperation related to primary surgery other than re-excision.
Shoulder function
Assessed using the Disability of the Arm, Shoulder and Hand (DASH) questionnaire. Higher scores mean a worse outcome.
Post-operative pain
Assessed using the visual analogue scale (VAS). Scale 1-10, higher scores mean a worse outcome.
Post-operative pain
Post-operative use of analgesics (paracetamol, NSAID's, opioids).
Cosmetic outcome assessed by an independent panel
an independent panel of four surgeons will blindly assess cosmetics by classifying standardised digital photographs one a 4-point Likert scale with the following categories: poor, fair, good and excellent. Photos are taken in two positions: the first in neutral position with both arms hanging next to the body and the second with both arms raised in 180gr (or as far as possible) elevation.
Patient reported satisfaction with breast
BreastQ questionnaire for mastectomy

Full Information

First Posted
December 30, 2021
Last Updated
March 8, 2022
Sponsor
Canisius-Wilhelmina Hospital
Collaborators
Rijnstate Hospital, OLVG, Martini Hospital Groningen, Catharina Ziekenhuis Eindhoven, St Jansdal Hospital, Bravis Hospital, Diakonessenhuis, Utrecht, St. Antonius Hospital, Gelderse Vallei Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05272904
Brief Title
The QUILT Study: Quilting Sutures in Patients Undergoing Breast Cancer Surgery
Acronym
QUILT
Official Title
The QUILT Study: Quilting Sutures in Patients Undergoing Breast Cancer Surgery: a Stepped Wedge Cluster Randomized Trial Study
Study Type
Interventional

2. Study Status

Record Verification Date
March 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
August 1, 2022 (Anticipated)
Primary Completion Date
January 1, 2023 (Anticipated)
Study Completion Date
July 1, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Canisius-Wilhelmina Hospital
Collaborators
Rijnstate Hospital, OLVG, Martini Hospital Groningen, Catharina Ziekenhuis Eindhoven, St Jansdal Hospital, Bravis Hospital, Diakonessenhuis, Utrecht, St. Antonius Hospital, Gelderse Vallei Hospital

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
Seroma is the most common complication following breast cancer surgery, with reported incidence up to 90%. Seroma causes patient discomfort, is associated with surgical site infections (SSI), often requires treatment and increases healthcare consumption. The quilting technique, in which the skin flaps are sutured to the pectoralis muscle, leads to a significant reduction of seroma with a decrease in the number of aspirations and surgical site infections. Main objective of this randomized stepped wedge study is to assess the impact of large scale implementation of the quilting technique in patients undergoing mastectomy and/or axillary lymph node dissection. This will be one of the first multicentre prospective studies in which quilting without postoperative wound drain is compared with conventional wound closure. The hypothesis is that quilting is a simple and cost-effective technique to increase textbook outcome. Moreover, it is expected that patient comfort is enhanced by quilting.
Detailed Description
Seroma is the most common complication following breast cancer surgery, with reported incidence up to 90%. Seroma causes patient discomfort, is associated with surgical site infections (SSI), often requires treatment and increases healthcare consumption. The quilting technique, in which skin flaps are sutured to the pectoralis muscle, leads to a significant reduction of seroma with a decrease in the number of aspirations and surgical site infections. However, implementation is lagging due to unknown side effects, increase in operation time and cost effectiveness. Main objective of this study is to assess the impact of large scale implementation of the quilting suture technique in patients undergoing mastectomy and/or axillary lymph node dissection (ALND). The QUILT study is a stepped wedge design study performed among nine teaching hospitals in the Netherlands. The study consists of nine steps, with each step one hospital will implement the quilting suture technique. Allocation of the order of implementation will be randomization-based. Primary outcome is 'textbook outcome', i.e.no wound complications, no re-admission, re-operation or unscheduled visit to the outpatient clinic and use of analgesics is not increased postoperative. A total of 113 patients is required based on a sample size calculation. This will be one of the first multicentre prospective studies in which quilting without postoperative wound drain is compared with conventional wound closure. The hypothesis is that quilting is a simple technique to increase textbook outcome, without increasing health care consumption. Moreover, the expectation is that patient comfort is enhanced by quilting.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Seroma
Keywords
Mastectomy, Breast cancer surgery, Quilting, Flap fixation, Seroma, Complications, Shoulder function, Pain, Cosmetic outcome, Health care consumption

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The QUILT study is a stepped wedge cluster randomized study.
Masking
None (Open Label)
Masking Description
Surgical technique is not blinded for surgeon and/or patients. An independent panel of four surgeons will blindly assess cosmetics.
Allocation
Randomized
Enrollment
113 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Conventional closure method
Arm Type
Active Comparator
Arm Description
Following mastectomy, skin is closed using subcutaneous sutures followed by intracutaneous running suture. Depending on the surgeons discretion a vacuum closed suction drain was placed beneath the skin flaps.
Arm Title
Quilting
Arm Type
Experimental
Arm Description
The implemented intervention is the quilting suture technique. The subcutaneous tissue is sutured to the pectoralis muscle placing multiple rows of running sutures. The suture starts at either end of the scar, running back and forth, creating rows of quilting stiches. The rows are placed transversely from the cranial to the caudal end of the wound with 2-3 cm between them, totalling some three to five rows for the cranial flap. The caudal flap is quilted with 2-3 rows in a caudal to cranial fashion. A subcutaneous suture followed by a intracutaneous running suture is used to close the skin. No wound drain is placed.
Intervention Type
Procedure
Intervention Name(s)
Quilting
Intervention Description
Following mastectomy and/or axillary lymph node dissection, the subcutaneous tissue is sutured to the pectoralis muscle placing multiple rows of running sutures. The suture starts at either end of the scar, running back and forth, creating rows of quilting stiches. The rows are placed transversely from the cranial to the caudal end of the wound with 2-3 cm between them, totalling some three to five rows for the cranial flap. The caudal flap is quilted with 2-3 rows in a caudal to cranial fashion. A subcutaneous suture followed by a intracutaneous running suture is used to close the skin.
Intervention Type
Procedure
Intervention Name(s)
Conventional wound closure
Intervention Description
Following mastectomy, skin is closed using subcutaneous sutures followed by intracutaneous running suture. Depending on the surgeons discretion a vacuum closed suction drain was placed beneath the skin flaps.
Primary Outcome Measure Information:
Title
Textbook outcome
Description
'Textbook outcome' (TO), a combination of outcome parameters reflecting an ideal surgical outcome. Measured 6 months post-operative, the patients postoperative course must comply with the following to meet the definition of TO: no wound complications no re-admissions in relation to primary surgery no re-operation in relation to primary surgery, re-excisions in case of involved margins allowed no unscheduled visit to the outpatient clinic (depending on the centre one or two postoperative visits are usually scheduled) postoperative use of analgesics (6 months) is not increased compared to pre-operative
Time Frame
6 months
Secondary Outcome Measure Information:
Title
All palpation-detected seromas
Description
Severity of complicaties are scored using the Clavien Dindo Classification of Surgical complications (grade I-V).
Time Frame
6 months
Title
Clinical significant seroma
Description
All aspirated seroma. Severity of complicaties are scored using the Clavien Dindo Classification of Surgical complications (grade I-V).
Time Frame
6 months
Title
Surgical site infections
Description
Severity of complicaties are scored using the Clavien Dindo Classification of Surgical complications (grade I-V).
Time Frame
6 months
Title
Bleeding complications
Description
Severity of complicaties are scored using the Clavien Dindo Classification of Surgical complications (grade I-V).
Time Frame
6 months
Title
Wound healing problems
Description
Including skin flap necrosis, wound necrosis, wound dehiscence. Severity of complicaties are scored using the Clavien Dindo Classification of Surgical complications (grade I-V).
Time Frame
6 months
Title
Duration of surgery
Description
Duration of surgery in minutes.
Time Frame
360 minutes
Title
Length of hospital stay
Description
Length of hospital stay in days: distinguishing between outpatient and inpatient treatment.
Time Frame
6 months
Title
Unscheduled visits to the outpatient clinic
Description
Number of unscheduled visits to the outpatient clinic
Time Frame
6 months
Title
Readmission to the hospital
Description
Readmission to the hospital related to primary surgery
Time Frame
6 months
Title
Reoperation
Description
Reoperation related to primary surgery other than re-excision.
Time Frame
6 months
Title
Shoulder function
Description
Assessed using the Disability of the Arm, Shoulder and Hand (DASH) questionnaire. Higher scores mean a worse outcome.
Time Frame
6 months
Title
Post-operative pain
Description
Assessed using the visual analogue scale (VAS). Scale 1-10, higher scores mean a worse outcome.
Time Frame
14 days
Title
Post-operative pain
Description
Post-operative use of analgesics (paracetamol, NSAID's, opioids).
Time Frame
6 months
Title
Cosmetic outcome assessed by an independent panel
Description
an independent panel of four surgeons will blindly assess cosmetics by classifying standardised digital photographs one a 4-point Likert scale with the following categories: poor, fair, good and excellent. Photos are taken in two positions: the first in neutral position with both arms hanging next to the body and the second with both arms raised in 180gr (or as far as possible) elevation.
Time Frame
6 months
Title
Patient reported satisfaction with breast
Description
BreastQ questionnaire for mastectomy
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: all patients >18 years of age undergoing mastectomy and/or axillary lymph node dissection be irrespective of the nature of the primary tumour: prophylactic, risk reducing, benign, in situ carcinoma and invasive primary or recurrent carcinoma will be eligible, irrespective of preoperative systemic therapy. Exclusion Criteria: patients who objected to participation (letter of objection) mentally incompetent patients or otherwise unable to complete a questionnaire immediate breast reconstruction pregnancy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Lotte van Zeelst, MS
Phone
0031681515149
Email
l.vanzeelst@cwz.nl
First Name & Middle Initial & Last Name or Official Title & Degree
Luc Strobbe, PhD
Email
ljastrobbe@cwz.nl
Facility Information:
Facility Name
Canisius Wilhelmina Hospital
City
Nijmegen
State/Province
Gelderland
ZIP/Postal Code
6532 SZ
Country
Netherlands

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
The datasets used and/or analysed during the study are available from the first and senior author on reasonable request.

Learn more about this trial

The QUILT Study: Quilting Sutures in Patients Undergoing Breast Cancer Surgery

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