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临床试验/NCT05941351
NCT05941351尚未招募不适用

fixAtion of skiN Flaps After Mastectomy Using ruNning or Interrupted suturEs for Combatting Seroma

Zuyderland Medisch Centrum2 个研究点 分布在 1 个国家目标入组 361 人开始时间: 2025年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
361
试验地点
2
主要终点
Complications requiring an intervention

研究概览

简要总结

Rationale: Flap fixation significantly reduces the incidence of seroma formation after mastectomy. Therefore, research should focus on finding the most optimal way to secure the skin flaps to the pectoral muscle. Previous studies have compared running sutures, interrupted sutures and tissue glue application to conventional wound closure. A recent systematic review with network meta-analysis indicated running sutures as the most optimal technique, however direct comparisons and high quality articles were lacking.

Objective: This prospective trial aims to directly compare running sutures with interrupted sutures in order to prevent complications in patients undergoing a mastectomy.

Study design: This trial will combine a retrospective cohort from the previous SARA-trial in Zuyderland MC with a randomised prospective trial. This study design was chosen to acquire a sample size with sufficient power and the ability to conduct this study in an acceptable time frame.

Study population: A retrospective cohort of patients participating in the SARA trial (RCT) and a prospective cohort of patients undergoing a mastectomy for breast cancer.

Intervention: Group 1: Flap fixation after mastectomy with running sutures. Group 2: Flap fixation after mastectomy with interrupted sutures.

Main study parameters/endpoints: The primary endpoint is the incidence of complications requiring interventions in both groups, including clinically significant seroma, infections and bleeding complications. Secondarily, the length of the procedure and cosmetic results will be compared.

Nature and extent of the burden and risks associated with participation, benefit and group relatedness: When participating, patients will undergo 3 additional outpatient clinic visits. Study visits will be combined with regular visits where possible, including the first postoperative visit after 7-10 days and either the 6 week or 3 month visit.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

性别
Female
接受健康志愿者

入选标准

  • Female sex.
  • 18 years or older.
  • Indication for mastectomy.

排除标准

  • Patients undergoing breast conserving therapy
  • Patients undergoing direct breast reconstruction
  • Patients undergoing modified radical mastectomy
  • Unable to comprehend implications and extent of study and sign for informed consent

结局指标

主要结局

Complications requiring an intervention

时间窗: 3 months

The main study parameter is the incidence of complications requiring interventions in both groups. This consists of: * Clinically significant seroma, requiring aspirations in the case of: * Pain or discomfort for the patient caused by large amounts of seroma characterised by tenderness of the skin. * Signs of infection (redness, swelling, pain). * Signs of delayed wound healing (wound breakdown, necrosis, seroma leakage). * Surgical site infections, requiring oral/iv antibiotics or surgical drainage. * Bleeding complications, requiring re-intervention, aspiration or surgical debridement.

次要结局

  • Cosmetic outcome(3 months)
  • Surgery time(during surgery)

研究者

发起方
Zuyderland Medisch Centrum
申办方类型
Other
责任方
Sponsor

研究点 (2)

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