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People's Hospital of Xinjiang Uygur Autonomous Region

2026年5月25日 更新者:Xiumin Zhang、People's Hospital of Xinjiang Uygur Autonomous Region

Objective: To evaluate the impact of enhanced recovery after surgery (ERAS)-based nursing intervention on venous thromboembolism (VTE) and lymphedema after radical hysterectomy for cervical cancer.

Methods: In this prospective randomized controlled trial, 160 patients scheduled for radical hysterectomy during September 2022-September 2024 were randomized to an ERAS group (n = 80) or a control group (n = 80). The control group received conventional perioperative care, while the ERAS group received a multimodal perioperative care protocol. Primary outcomes were the 6-month incidence of VTE and lower limb lymphedema. Secondary outcomes included recovery indicators, inflammatory and coagulation markers, quality of life [QoL; assessed by the Quality of Life Questionnaire-Core 30 (QLQ-C30)], and nursing satisfaction.

研究概览

研究类型

介入性

注册 (实际的)

160

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Xinjiang Uygur Autonomous Region
      • Ürümqi、Xinjiang Uygur Autonomous Region、中国、830000
        • People's Hospital of Xinjiang Uygur Autonomous Region

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

  • . Pathologically confirmed cervical cancer (FIGO 2018) 2. Age 18-70 years 3. First-time radical hysterectomy 4. ASA physical status class I-II 5. Perioperative anticoagulant prophylaxis per hospital standards 6. Provision of informed consent

Exclusion Criteria:

  • 1. Pre-existing lower extremity DVT, lymphedema, or severe varicose veins 2. Severe cardiac, hepatic, or renal dysfunction or coagulation disorders 3. History of psychiatric illness or communication barriers 4. Pregnant or lactating women

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:支持治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
无干预:Conventional Perioperative Care
The control group received conventional perioperative care. This included routine preoperative education, fasting for 12 hours and no oral intake for 6 hours preoperatively, standard intraoperative fluid administration, postoperative patient-controlled analgesia pump, ambulation guided by traditional instructions (typically 1-2 days postoperatively), and initiation of liquid diet after passing flatus.
实验性的:ERAS Multimodal Pathway

In addition to conventional care, the ERAS group received a comprehensive intervention protocol based on ERAS principles, implemented by a dedicated ERAS nursing team. Details are as follows:

Preoperative interventions: (1) Enhanced education and prehabilitation: Detailed explanation of the ERAS pathway, VTE and lymphedema prevention using graphics and videos. Instruction on ankle pump exercises and quadriceps isometric contractions. (2) Nutritional support: Nutritional risk assessment and provision of oral nutritional supplements if necessary. (3) Fasting management: No solid food for 6 hours, clear oral fluids (e.g., 200 mL of 10% glucose solution) allowed up to 2 hours preoperatively.

Intraoperative interventions: (1) Thermoregulation: Use of forced-air warming blankets and fluid warmers to maintain core temperature > 36°C. (2) Restrictive fluid management: Goal-directed fluid therapy to avoid excessive infusion. (3) Minimally invasive and meticulous surgery: Encouragement of lapar

In addition to conventional care, the ERAS group received a comprehensive intervention protocol based on ERAS principles, implemented by a dedicated ERAS nursing team. Details are as follows:

Preoperative interventions: (1) Enhanced education and prehabilitation: Detailed explanation of the ERAS pathway, VTE and lymphedema prevention using graphics and videos. Instruction on ankle pump exercises and quadriceps isometric contractions. (2) Nutritional support: Nutritional risk assessment and provision of oral nutritional supplements if necessary. (3) Fasting management: No solid food for 6 hours, clear oral fluids (e.g., 200 mL of 10% glucose solution) allowed up to 2 hours preoperatively.

Intraoperative interventions: (1) Thermoregulation: Use of forced-air warming blankets and fluid warmers to maintain core temperature > 36°C. (2) Restrictive fluid management: Goal-directed fluid therapy to avoid excessive infusion. (3) Minimally invasive and meticulous surgery: Encouragement of laparo

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Incidence of Postoperative Venous Thromboembolism (VTE)
大体时间:6 months after surgery
Composite incidence of deep vein thrombosis (DVT) of the lower extremities and pulmonary embolism (PE). DVT is diagnosed by bilateral lower extremity venous color Doppler ultrasonography performed on postoperative day 3, before discharge, and at 1, 3, and 6 months postoperatively or when clinically indicated. PE is evaluated by computed tomography pulmonary angiography (CTPA) when clinically suspected.
6 months after surgery

次要结果测量

结果测量
措施说明
大体时间
Incidence of Postoperative Lower Limb Lymphedema
大体时间:6 months after surgery
Diagnosis based on International Society of Lymphology criteria (Grade I: pitting edema relieved by elevation; Grade II: non-pitting edema with tissue fibrosis; Grade III: elephantiasis). Measured by bilateral calf circumference (thickest point) and thigh circumference (15 cm above patella).
6 months after surgery
Time to First Flatus
大体时间:Within 14 days after surgery (typically hours to days)
Number of hours from surgery completion to first passage of flatus, indicating recovery of gastrointestinal function.
Within 14 days after surgery (typically hours to days)
Time to First Defecation
大体时间:Within 14 days after surgery (typically days)
Number of hours from surgery completion to first bowel movement.
Within 14 days after surgery (typically days)
Time to First Ambulation
大体时间:Within 7 days after surgery
Number of days from surgery completion to the first time the patient walks independently (assisted or unassisted) outside the bed area.
Within 7 days after surgery
Postoperative Length of Hospital Stay
大体时间:At hospital discharge, assessed up to 4 weeks postoperatively
Total number of days from the date of surgery to the date of hospital discharge.
At hospital discharge, assessed up to 4 weeks postoperatively
Change in C-Reactive Protein (CRP)
大体时间:Preoperative (baseline) vs. Postoperative day 3
Change in serum C-reactive protein (CRP) measured from fasting blood samples, reported in mg/L.
Preoperative (baseline) vs. Postoperative day 3
Change in D-Dimer (D-D)
大体时间:Preoperative (baseline) vs. Postoperative day 3
Change in plasma D-dimer (D-D) measured from fasting blood samples, reported in mg/L.
Preoperative (baseline) vs. Postoperative day 3
Change in Platelet Count (PLT)
大体时间:Preoperative (baseline) vs. Postoperative day 3
Change in platelet count (PLT) measured from complete blood count, reported in ×10⁹/L.
Preoperative (baseline) vs. Postoperative day 3
Change in Global Health Status / Quality of Life (QLQ-C30)
大体时间:Preoperative (baseline) vs. 6 months postoperatively
Change in the Global Health Status / Quality of Life subscale score from the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30). Minimum value: 0. Maximum value: 100. Higher scores indicate better quality of life.
Preoperative (baseline) vs. 6 months postoperatively
Nursing Satisfaction
大体时间:At hospital discharge (postoperative day 7 to day 15)
Measured by the Newcastle Satisfaction with Nursing Scale (NSNS). Categorized as: highly satisfied, moderately satisfied, or not satisfied. Overall satisfaction rate = (highly satisfied + moderately satisfied) / total patients × 100%.
At hospital discharge (postoperative day 7 to day 15)
Change in White Blood Cell Count (WBC)
大体时间:Preoperative (baseline) vs. Postoperative day 3
Change in white blood cell count (WBC) measured from fasting blood samples, reported in ×10⁹/L.
Preoperative (baseline) vs. Postoperative day 3
Change in Prothrombin Time (PT)
大体时间:Preoperative (baseline) vs. Postoperative day 3
Change in prothrombin time (PT) measured from fasting blood samples, reported in seconds.
Preoperative (baseline) vs. Postoperative day 3
Change in Hemoglobin (Hb)
大体时间:Preoperative (baseline) vs. Postoperative day 3
Change in hemoglobin (Hb) measured from complete blood count, reported in g/L.
Preoperative (baseline) vs. Postoperative day 3
Change in Functional Scales (QLQ-C30)
大体时间:Preoperative (baseline) vs. 6 months postoperatively
Change in the Functional Scales composite score from the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30). Minimum value: 0. Maximum value: 100. Higher scores indicate better functional status.
Preoperative (baseline) vs. 6 months postoperatively
Change in Symptom Scales (QLQ-C30)
大体时间:Preoperative (baseline) vs. 6 months postoperatively
Change in the Symptom Scales composite score from the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30). Minimum value: 0. Maximum value: 100. Higher scores indicate worse symptom burden.
Preoperative (baseline) vs. 6 months postoperatively
Change in Single Items (QLQ-C30)
大体时间:Preoperative (baseline) vs. 6 months postoperatively
Change in the Single Items score (including dyspnea, insomnia, appetite loss, constipation, diarrhea, financial difficulties) from the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30). Minimum value: 0. Maximum value: 100. Higher scores indicate worse symptom burden or greater financial difficulty.
Preoperative (baseline) vs. 6 months postoperatively
Change in Total Score (QLQ-C30)
大体时间:Preoperative (baseline) vs. 6 months postoperatively
Change in the total score from the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30). Minimum value: 0. Maximum value: 100. Higher scores indicate better overall quality of life.
Preoperative (baseline) vs. 6 months postoperatively

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2022年9月5日

初级完成 (实际的)

2024年9月17日

研究完成 (实际的)

2024年9月26日

研究注册日期

首次提交

2026年5月19日

首先提交符合 QC 标准的

2026年5月25日

首次发布 (实际的)

2026年5月29日

研究记录更新

最后更新发布 (实际的)

2026年5月29日

上次提交的符合 QC 标准的更新

2026年5月25日

最后验证

2026年5月1日

更多信息

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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