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Study Comparing Negative Pressure Dressing vs Conventional in Patients With Resected STS After Radiotherapy (TPN-RAD)

Primary Purpose

Soft Tissue Sarcoma

Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Prevena
Sponsored by
Centre Leon Berard
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Soft Tissue Sarcoma focused on measuring STS, Negative Pressure Wound Therapy, Surgery with preoperative irradiation

Eligibility Criteria

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

Inclusion Criteria: Age ≥ 18 years at the day of consenting to the study Patients with primary STS of the limb or trunk treated with preoperative external radiation therapy (decided in multidisciplinary board) Intent to cure resection required for STS planned between 3 to 8 weeks after the end of RT Planned primary wound closure, including local or distant jambeau Ability to understand and willingness for follow-up visits Covered by a medical insurance Signed and dated informed consent document indicating that the patient has been informed of all aspects of the trial prior to enrolment. Exclusion Criteria: Known hypersensibility to silver Patients with a diagnosis of Ewing's sarcoma, chondrosarcoma, osteosarcoma, or desmoid tumor Planned no wound-closure and skin graft after resection Patient requiring authorship or curators or patient deprived of liberty.

Sites / Locations

  • CHU Nantes
  • Centre Leon BerardRecruiting
  • Institut Bergonié
  • CHRU Tours Hôpital Trousseau
  • Centre Jean Perrin
  • Centre Georges François Leclerc
  • Centre Oscar Lambert
  • CHU Limoges
  • Institut du Cancer de Montpellier
  • Institut Curie
  • APHP Hôpital Cochin
  • CHU Rennes
  • IUCT Oncopole

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Arm A : Surgery for STS and prevena

Arm B : Surgery for STS and standard postoperative wound management

Arm Description

The surgery for the STS lesion will be performed according to standard practices. PREVENA™ Incision Management System should be applied immediately post-surgery to clean surgically closed wounds. It should be continuously applied for a minimum of 2 days and up to a maximum of 7 days (as per PREVENA user manual)

The surgery for the STS lesion will be performed according to standard practices. The dressing and drainage of the wound will be performed according to usual practices, with the exception of negative pressure dressings.

Outcomes

Primary Outcome Measures

The efficacy of negative pressure therapy (PREVENA) versus standard postoperative wound management on the wound healing after surgery for previously irradiated STS
Assessed by major wound complications rate

Secondary Outcome Measures

Three month deep infection rate
Assessed by the proportion of patients experiencing a second surgery for wound healing problem within 3 postoperative months
Three months secondary surgery for wound healing problem rate
Assessed by the proportion of patients experiencing a second surgery for wound healing problem within 3 postoperative months
Hospitalization duration
Defined as the number of hospitalization days from the date of surgery to the date of discharge
Time to complete wound healing
Defined as the interval from surgery to 100% healing (total wound closure with no need for dressing and any local care)
Number and types of major wound complications (MWCs)
Assessed by a number and differens types of a major wound complications
Quality of life using EQ-5D-5L
Assessed by EQ-5D-5L introduce by EuroQol Group in 2009 with five dimensions : mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has five levels : no problems, slight problems, moderate problems, severe problems and extreme problems. A minimum value is 0 and a maximum value is 100. A mean worst value is 0 and a better mean value is 100.
Incidence of Adverse Events
Defined by the number of patients with Adverse Events (any type and any grade using the NCI-CTC AE scale version 5.0)
Quality of life using FACT-G
Assessed by FACT-G : Functionnal Assesment of Cancer Therapy with 27 items. There are four domains of HRQOL in cancer patients: Physical, social, emotional, and functional well-being. A minimum value is 0 and a maximum value is 4. A mean worst value is 0 and a better mean value is 108.

Full Information

First Posted
June 26, 2023
Last Updated
August 31, 2023
Sponsor
Centre Leon Berard
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1. Study Identification

Unique Protocol Identification Number
NCT05944913
Brief Title
Study Comparing Negative Pressure Dressing vs Conventional in Patients With Resected STS After Radiotherapy
Acronym
TPN-RAD
Official Title
Randomized Study Comparing Negative Pressure Dressing Versus Conventional Dressing in Patients With Resected Limb or Trunk Soft Tissue Sarcoma (STS) After External Radiotherapy
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
August 3, 2023 (Actual)
Primary Completion Date
August 2025 (Anticipated)
Study Completion Date
August 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Leon Berard

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 is a randomized (1:1 ratio), prospective, comparative, controlled, open-label study. The aim is to compare the efficacy of negative pressure therapy (PREVENA™) versus standard postoperative wound management on the wound healing after surgery for previously irradiated Soft Tissue Sarcoma (STS)
Detailed Description
The gold standard treatment for primary non-metastatic STS is complete surgical resection. Peri-operative Radiation Therapy (RT) has been proved to improve local control . Nevertheless, the timing of RT, whether preoperative or postoperative, remains a debate. Both have similar local control efficacy, but preoperative RT results in lower rates of long-term fibrosis and lymphedema and improved joint mobility than postoperative RT. On the other hand, the adverse effect of pre-operative RT is a higher rate of wound post-operative complications and re-operations. Any effort to reduce the high rate of postoperative complications could offer the advantage of preoperative RT in terms of reduced long-term sequelae compared with postoperative RT without a higher wound complication rate postoperatively. Short retrospective series of Negative Pressure Wound Therapy (NPWT) after surgical resection of Soft Tissue Sarcoma (STS) have reported very encouraging results in preventing wound complications: patients treated with NPWT were less likely to develop wound complications than those who did not receive it. Both groups did not report an increased rate of local recurrence. The use of NPWT would also reduce the cost of care by avoiding complications. That's why the investigators propose this study comparing the use of a negative pressure dressing to a conventional dressing in patients with STS of the limbs or trunk resected after neo-adjuvant external radiotherapy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Soft Tissue Sarcoma
Keywords
STS, Negative Pressure Wound Therapy, Surgery with preoperative irradiation

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The randomization (1:1 ratio) will be stratified according to STS location (upper limb vs lower limb vs trunk) and ASA class (1 or 2 vs ≥ 3).
Masking
None (Open Label)
Allocation
Randomized
Enrollment
166 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Arm A : Surgery for STS and prevena
Arm Type
Experimental
Arm Description
The surgery for the STS lesion will be performed according to standard practices. PREVENA™ Incision Management System should be applied immediately post-surgery to clean surgically closed wounds. It should be continuously applied for a minimum of 2 days and up to a maximum of 7 days (as per PREVENA user manual)
Arm Title
Arm B : Surgery for STS and standard postoperative wound management
Arm Type
No Intervention
Arm Description
The surgery for the STS lesion will be performed according to standard practices. The dressing and drainage of the wound will be performed according to usual practices, with the exception of negative pressure dressings.
Intervention Type
Device
Intervention Name(s)
Prevena
Intervention Description
PREVENA™ is a CE-marked class IIa medical device. The PREVENA™ Incision Management System is also intended to manage the environment of closed surgical incisions and surround intact skin in patients at risk for developing post-operative complications, such as infection, by maintaining a closed environment via the application of a negative pressure wound therapy system to the incision.
Primary Outcome Measure Information:
Title
The efficacy of negative pressure therapy (PREVENA) versus standard postoperative wound management on the wound healing after surgery for previously irradiated STS
Description
Assessed by major wound complications rate
Time Frame
At 3 months post-surgery visit
Secondary Outcome Measure Information:
Title
Three month deep infection rate
Description
Assessed by the proportion of patients experiencing a second surgery for wound healing problem within 3 postoperative months
Time Frame
At 3 months post-surgery visit
Title
Three months secondary surgery for wound healing problem rate
Description
Assessed by the proportion of patients experiencing a second surgery for wound healing problem within 3 postoperative months
Time Frame
At 3 months post-surgery visit
Title
Hospitalization duration
Description
Defined as the number of hospitalization days from the date of surgery to the date of discharge
Time Frame
At 3 months post-surgery visit
Title
Time to complete wound healing
Description
Defined as the interval from surgery to 100% healing (total wound closure with no need for dressing and any local care)
Time Frame
Up to 27 months
Title
Number and types of major wound complications (MWCs)
Description
Assessed by a number and differens types of a major wound complications
Time Frame
Up to 27 months
Title
Quality of life using EQ-5D-5L
Description
Assessed by EQ-5D-5L introduce by EuroQol Group in 2009 with five dimensions : mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has five levels : no problems, slight problems, moderate problems, severe problems and extreme problems. A minimum value is 0 and a maximum value is 100. A mean worst value is 0 and a better mean value is 100.
Time Frame
At 28 days and 3 months after surgery for each patients
Title
Incidence of Adverse Events
Description
Defined by the number of patients with Adverse Events (any type and any grade using the NCI-CTC AE scale version 5.0)
Time Frame
Up to 27months
Title
Quality of life using FACT-G
Description
Assessed by FACT-G : Functionnal Assesment of Cancer Therapy with 27 items. There are four domains of HRQOL in cancer patients: Physical, social, emotional, and functional well-being. A minimum value is 0 and a maximum value is 4. A mean worst value is 0 and a better mean value is 108.
Time Frame
At 28 days and 3 months after surgery for each patients

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥ 18 years at the day of consenting to the study Patients with primary STS of the limb or trunk treated with preoperative external radiation therapy (decided in multidisciplinary board) Intent to cure resection required for STS planned between 3 to 8 weeks after the end of RT Planned primary wound closure, including local or distant jambeau Ability to understand and willingness for follow-up visits Covered by a medical insurance Signed and dated informed consent document indicating that the patient has been informed of all aspects of the trial prior to enrolment. Exclusion Criteria: Known hypersensibility to silver Patients with a diagnosis of Ewing's sarcoma, chondrosarcoma, osteosarcoma, or desmoid tumor Planned no wound-closure and skin graft after resection Patient requiring authorship or curators or patient deprived of liberty.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
François Gouin, MD, Chirurgien
Phone
0469855311
Ext
+33
Email
Francois.GOUIN@lyon.unicancer.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Séverine METZGER, Project Manager
Phone
0478782786
Ext
+33
Email
severine.metzger@lyon.unicancer.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
François Gouin, MD, Chirurgien
Organizational Affiliation
Centre Leon Berard
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHU Nantes
City
Nantes
State/Province
Pays De Loire
ZIP/Postal Code
44093
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
CRENN Vincent, MD,surger
Phone
0240083761
Ext
+33
Email
vincent.crenn@chu-nantes.fr
Facility Name
Centre Leon Berard
City
Lyon
State/Province
Rhône-Alpes Auvergne
ZIP/Postal Code
69008
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
GOUIN François, MD, surger
Phone
0469855311
Ext
+33
Email
francois.gouin@lyon.unicancer.fr
First Name & Middle Initial & Last Name & Degree
VAZ Gualter, MD, Surger
Phone
0469855310
Ext
+33
Email
gualter.vaz@lyon.unicancer.fr
Facility Name
Institut Bergonié
City
Bordeaux
ZIP/Postal Code
33076
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
MICHOT Audrey, MD,surger
Phone
0556333216
Email
a.michot@bordeaux.unicancer.fr
Facility Name
CHRU Tours Hôpital Trousseau
City
Chambray-lès-Tours
ZIP/Postal Code
37170
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
LE NAIL Louis-Romée, MD,surger
Email
lr.lenail@chu-tours.fr
Facility Name
Centre Jean Perrin
City
Clermont-Ferrand
ZIP/Postal Code
63011
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
GIMBERGUES Pierre, MD,surger
Phone
0473278000
Email
pierre.gimbergues@clermont.unicancer.fr
Facility Name
Centre Georges François Leclerc
City
Dijon
ZIP/Postal Code
21000
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
CAUSERET Sylvain, MD, surger
Email
scauseret@cgfl.fr
Facility Name
Centre Oscar Lambert
City
Lille
ZIP/Postal Code
59000
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
DECANTER Gauthier, MD,surger
Email
g-decanter@o-lambret.fr
Facility Name
CHU Limoges
City
Limoges
ZIP/Postal Code
87042
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
FIORENZA Fabrice, MD,surger
Email
fabrice.fiorenza@chu-limoges.fr
Facility Name
Institut du Cancer de Montpellier
City
Montpellier
ZIP/Postal Code
34090
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
CARRERE Sébastien, MD,surger
Phone
0467614539
Email
sebastien.carrere@icm.unicancer.fr
Facility Name
Institut Curie
City
Paris
ZIP/Postal Code
75005
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
TZANIS Dimitri, MD, surger
Email
dimitri.tzanis@curie.fr
Facility Name
APHP Hôpital Cochin
City
Paris
ZIP/Postal Code
75014
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
BIAU David, MD,surger
Email
david.biau@aphp.fr
Facility Name
CHU Rennes
City
Rennes
ZIP/Postal Code
35033
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
ROPARS Mickaël, MD,surger
Email
mickael.ropars@chu-rennes.fr
Facility Name
IUCT Oncopole
City
Toulouse
ZIP/Postal Code
31100
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
MERESSE Thomas, MD,surger
Phone
0531156032
Email
meresse.thomas@iuct-oncopole.fr

12. IPD Sharing Statement

Learn more about this trial

Study Comparing Negative Pressure Dressing vs Conventional in Patients With Resected STS After Radiotherapy

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