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临床试验/NCT07335432
NCT07335432Enrolling By Invitation不适用

Efficacy of Intravenous Vitamin C Versus Placebo on Estimated Blood Loss in Total Abdominal Hysterectomy

Queen Savang Vadhana Memorial Hospital, Thailand2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2024年9月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
Enrolling By Invitation
发起方
入组人数
40
试验地点
2
主要终点
Intraoperative estimate blood loss

研究概览

简要总结

Intervention Group: Received two 1 gm doses of Vitamin C intravenously (IV). first Dose: At midnight on the day of surgery. Second Dose: Immediately after the surgical incision. Control Group: Received two doses of a normal saline intravenously (IV) at the exact same times.

The primary outcome was to compare intraoperative blood loss between patients who received intravenous Vitamin C and those who did not, following an abdominal hysterectomy under general anesthesia.

Intraoperative estimated blood loss (EBL) was meticulously quantified by weighing surgical gauze and measuring suction canister volumes.

The secondary outcomes were to evaluate the potential benefits of Vitamin C administration, including:

  • Reduction in the decline of hematocrit levels after surgery.
  • Reduction of the length of hospital stay

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
Double (Participant, Investigator)

入排标准

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

入选标准

  • Female patients who underwent total abdominal hysterectomy
  • No bleeding tendency.
  • No history of anticoagulant or thrombolytic drug use
  • No contraindications to vitamin C supplementation

排除标准

  • Inability to communicate in the Thai language.
  • Underwent total abdominal hysterectomy due to gynecologic malignancy.
  • Required emergency total abdominal hysterectomy.
  • History of vitamin C supplementation within 2 weeks prior to surgery.
  • History of smoking.
  • Previous abdominal surgery, such as bowel surgery, cesarean section

研究组 & 干预措施

Experimental: Vitamin C

Experimental

Intervention Group: Received two 1 gm doses of Vitamin C intravenously (IV). first Dose: At midnight on the day of surgery. Second Dose: Immediately after the surgical incision. Control Group: Received two doses of a normal saline intravenously (IV) at the exact same times.

干预措施: Vitamin C (Ascorbic Acid) (Dietary Supplement)

Placebo

Experimental

干预措施: Vitamin C (Ascorbic Acid) (Dietary Supplement)

结局指标

主要结局

Intraoperative estimate blood loss

时间窗: intraoperative

次要结局

未报告次要终点

研究者

发起方
Queen Savang Vadhana Memorial Hospital, Thailand
申办方类型
Other
责任方
Principal Investigator
主要研究者

Aektanat Tawornkitpanich

M.D.

Queen Savang Vadhana Memorial Hospital, Thailand

研究点 (2)

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