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临床试验/NCT07368218
NCT07368218尚未招募不适用

Randomized Clinical Trial on Morbidity, Psychological Impact, and Changes in Biomarker Concentration During the Perioperative Period Comparing Transmesocolic Versus Retromesenteric Reconstruction in Cephalic Duodenopancreatectomy (FAST Trial)

Hospital Universitari de Bellvitge1 个研究点 分布在 1 个国家目标入组 124 人开始时间: 2026年1月31日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
124
试验地点
1
主要终点
Delayed Gastric Emptying

研究概览

简要总结

Objective: To compare the incidence of delayed gastric emptying (ISGPS 2007 criteria) between patients undergoing retromesenteric versus transmesocolic reconstruction after pancreaticoduodenectomy. Secondary objectives include evaluating overall postoperative morbidity (Clavien-Dindo ≥ Grade I) at 90 days, postoperative pancreatic fistula according to ISGPF criteria, 30- and 90-day mortality, differences in operative time and blood loss, hospital stay duration, exploratory analysis of inflammatory biomarkers in serum and drainage fluid, psychological impact using SCL-90-R scale, and postoperative quality of life using EORTC QLQ-C30 scale.

Methods: Randomized, controlled, single-center superiority clinical trial with 1:1 allocation. One hundred twenty-four patients candidates for duodenopancreatectomy due to pancreatic pathology will be randomized using balanced blocks to transmesocolic (control) or retromesenteric (study) reconstruction. Randomization will be revealed after completing the resection phase. Primary intention-to-treat analysis will estimate relative risk with 95% CI for dichotomous variables, Kaplan-Meier survival analysis with log-rank test, and linear mixed models for repeated measures in quality of life outcomes. Follow-up will be 90 days for the primary endpoint, extending to 12 months for secondary objectives.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age ≥ 18 years
  • Candidates for cephalic duodenopancreatectomy due to pancreatic pathology
  • Ability to complete follow-up questionnaires

排除标准

  • Emergency surgery
  • Participation in another clinical trial
  • Pregnancy or lactation
  • Severe psychiatric disorder that prevents follow-up
  • Inability to understand the information and sign study consent

研究组 & 干预措施

Transmesocolic reconstruction

Active Comparator

干预措施: Transmesocolic reconstruction (Procedure)

Retromesenteric reconstruction

Experimental

干预措施: Retromesenteric reconstruction (Procedure)

结局指标

主要结局

Delayed Gastric Emptying

时间窗: From first postoperative day to 30 days

Delayed gastric emptying according to ISGPS 2007 definition: Grade A (nasogastric tube \>3 days or reinsertion between days 4-7 + vomiting); Grade B (tube \>7 days or reinsertion after day 7 + vomiting); Grade C (impossibility of oral tolerance after day 14)

次要结局

  • Postoperative morbility(Form first postoperative day to day 30)
  • Pancreatic fistula(From first postoperative day to day 30)
  • Mortality(From first postoperative day to day 90)
  • Hospital stay(From first postoperative day to hospital discharge up to 15 weeks)
  • Operative time(Periprocedural time, an average time of 300-400 minutes)
  • Proportion of patients with NLR index ≥5(From the first postoperative day to one year follow-up)
  • Proportion of patients with CA19.9 >37 U/ml(From the first postoperative day to one year follow-up)
  • Cytokines in serum(From the first postoperative day to day 90)
  • Cytokines in abdominal drainage(From the first postoperative day to day 90)
  • Cytokines and complications correlation(From the first postoperative day to day 90)
  • Recurrence(From the first postoperative day to one year follow-up)
  • Time to recurrence(From the first postoperative day to one year follow-up)
  • Complications-recurrence correlation(From the first postoperative day to one year follow-up)

研究者

发起方
Hospital Universitari de Bellvitge
申办方类型
Other
责任方
Principal Investigator
主要研究者

BUSQUETS, JULI

Head of Pancreatic Surgery Unit

Hospital Universitari de Bellvitge

研究点 (1)

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