방사선 치료 후 절제된 STS 환자에서 음압 드레싱과 기존의 드레싱을 비교하는 연구 (TPN-RAD)
외부 방사선 요법 후 절제된 사지 또는 체간 연조직 육종(STS) 환자에서 음압 드레싱과 기존 드레싱을 비교하는 무작위 연구
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)
연구 개요
상세 설명
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.
연구 유형
등록 (실제)
단계
- 해당 없음
연락처 및 위치
연구 장소
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Angers, 프랑스, 49055
- Institut de Cancérologie de l'Ouest - Pays de Loire
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Bordeaux, 프랑스, 33076
- Institut Bergonié
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Chambray-lès-Tours, 프랑스, 37170
- CHRU Tours Hôpital Trousseau
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Clermont-Ferrand, 프랑스, 63011
- Centre Jean Perrin
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Dijon, 프랑스, 21000
- Centre Georges François Leclerc
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Lille, 프랑스, 59000
- Centre Oscar Lambert
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Limoges, 프랑스, 87042
- CHU Limoges
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Montpellier, 프랑스, 34090
- Institut du Cancer de Montpellier
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Paris, 프랑스, 75014
- APHP Hôpital Cochin
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Rennes, 프랑스, 35033
- CHU Rennes
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Toulouse, 프랑스, 31100
- IUCT Oncopole
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Vandœuvre-lès-Nancy, 프랑스, 54519
- Institut de Cancérologie de Lorraine
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Pays de Loire
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Nantes, Pays de Loire, 프랑스, 44093
- CHU Nantes
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Rhône-Alpes Auvergne
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Lyon, Rhône-Alpes Auvergne, 프랑스, 69008
- Centre Leon Berard
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
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. Nota bene: Only patients with bone tumors are affected; patients with soft tissue tumors can be included in the study.
- Patient in relapse setting;
- Patient requiring a surgical revision after R1 or R2 resection;
- Planned blade drainage;
- Planned no wound-closure and skin graft after resection
- Patient requiring authorship or curators or patient deprived of liberty.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 다른
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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실험적: Arm A : Surgery for STS and prevena
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) |
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. |
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간섭 없음: Arm B : Surgery for STS and standard postoperative wound management
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. |
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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The efficacy of negative pressure therapy (PREVENA) versus standard postoperative wound management on the wound healing after surgery for previously irradiated STS
기간: Within the 3-month postoperative period.
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Assessed by major wound complications rate |
Within the 3-month postoperative period.
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Three month deep infection rate
기간: At 3 months post-surgery visit
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Assessed by the proportion of patients experiencing a second surgery for wound healing problem within 3 postoperative months |
At 3 months post-surgery visit
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Three months secondary surgery for wound healing problem rate
기간: At 3 months post-surgery visit
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Assessed by the proportion of patients experiencing a second surgery for wound healing problem within 3 postoperative months |
At 3 months post-surgery visit
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Hospitalization duration
기간: At 3 months post-surgery visit
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Defined as the number of hospitalization days from the date of surgery to the date of discharge |
At 3 months post-surgery visit
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Time to complete wound healing
기간: Up to 27 months
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Defined as the interval from surgery to 100% healing (total wound closure with no need for dressing and any local care) |
Up to 27 months
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Number and types of major wound complications (MWCs)
기간: Up to 27 months
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Assessed by a number and differens types of a major wound complications |
Up to 27 months
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Quality of life using EQ-5D-5L
기간: At 28 days and 3 months after surgery for each patients
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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. |
At 28 days and 3 months after surgery for each patients
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Incidence of Adverse Events
기간: Up to 27months
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Defined by the number of patients with Adverse Events (any type and any grade using the NCI-CTC AE scale version 5.0) |
Up to 27months
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Quality of life using FACT-G
기간: At 28 days and 3 months after surgery for each patients
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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. |
At 28 days and 3 months after surgery for each patients
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공동 작업자 및 조사자
수사관
- 수석 연구원: François Gouin, MD, Chirurgien, Centre Leon Berard
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
기본 완료 (실제)
연구 완료 (실제)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
- ET22-146
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
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