Relationship Between Serum Estrogen Concentration and Propofol Injection Pain: A Prospective and Observational Study
概览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- Konya City Hospital
- 入组人数
- 90
- 试验地点
- 1
- 主要终点
- Incidence of Propofol Injection Pain
概览
简要总结
This prospective observational study investigates the relationship between serum estrogen concentration and the incidence and severity of propofol injection pain (PIP) in female patients undergoing general anesthesia. The study will include 90 ASA I-II female patients aged 18-45. One group will consist of IVF patients with elevated estrogen levels, while the control group will include patients with normal estrogen levels undergoing other elective procedures. Pain will be assessed using a standardized four-point behavioral pain scale. The findings may enhance understanding of hormonal influences on pain and contribute to improving patient comfort during anesthesia induction.
详细描述
This prospective observational study aims to evaluate the association between serum estrogen levels and the incidence and severity of propofol injection pain (PIP) in adult female patients undergoing general anesthesia. Although propofol is a widely used intravenous anesthetic, it frequently causes pain upon injection. Estrogen is believed to play a role in modulating pain perception and inflammatory responses, yet the effects of elevated estrogen levels on PIP are not well understood.
The study will be conducted at a single tertiary hospital and will include 90 ASA I-II female patients aged 18-45 years. One group will consist of IVF patients with elevated serum estradiol levels due to controlled ovarian stimulation. The control group will include patients with normal estradiol levels scheduled for elective procedures under general anesthesia. Preoperative serum estradiol levels will be recorded, and injection pain will be evaluated using a validated four-point behavioral pain scale based on vocal response, facial expression, limb movement, and tearfulness.
Anesthesia induction will follow standard clinical practice without additional interventions. Pain data will be collected through routine clinical observation. The results may offer new insights into hormonal modulation of acute nociceptive responses and help improve patient experiences during anesthesia.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 45 Years(Adult)
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Female patients aged between 18 and 45 years
- •American Society of Anesthesiologists (ASA) physical status I or II
- •Scheduled for surgery under general anesthesia
- •Availability of a preoperative serum estradiol (E2) level
- •For Group 1: Undergoing IVF procedure with supraphysiological E2 levels (\>350 pg/mL)
- •For Group 2: Undergoing elective surgery with normal E2 levels (15-350 pg/mL)
排除标准
- •ASA physical status III or IV
- •Pregnant patients
- •Perimenopausal women
- •Male patients
- •Patients younger than 18 or older than 45 years
- •History of psychiatric disorders
- •Patients undergoing emergency surgery
结局指标
主要结局
Incidence of Propofol Injection Pain
时间窗: Immediately during induction of anesthesia
Presence or absence of pain during propofol injection, assessed through patient response (verbal reaction, facial grimacing, arm withdrawal, or tearing) and/or verbal confirmation during anesthesia induction. Comparison between patients with normal and supraphysiological estradiol levels.
次要结局
- Severity of Propofol Injection Pain(Immediately during induction of anesthesia)
- Postoperative Injection Site Reactions(Within 24 hours after surgery)
研究者
Mahmut Sami TUTAR
Associate Professor, Department of Anesthesiology and Reanimation
Konya City Hospital