Comparison of three techniques in the management of the postoperatory acute pain, after a general anesthesia based on the control of the nociception.

Fundació Hospital Vall Hebron Institut de Recerca0 个研究点目标入组 204 人开始时间: 2016年8月11日最近更新: 2019年6月30日

适应症

试验速览

暂无简介。

•- Patients with ages between 18-75 years.
•- ASA I-II-III.
•- Body mass index (BMI ) less than 35 kg / m2 for women and 42 kg / m2 in men.
•- Major gynecological surgery abdominal hysterectomy laparoscopic or robotic radical prostatectomy.
•- Control Technology -TCI general anesthesia TIVA (total intravenous anesthesia by infusion systems controlled by computer).
•- Patients enroll in other clinical investigations can participate
•Are the trial subjects under 18? no
•Number of subjects for this age range:
•F.1.2 Adults (18-64 years) yes
•F.1.2.1 Number of subjects for this age range 154
•F.1.3 Elderly (>=65 years) yes
•F.1.3.1 Number of subjects for this age range 50

•- Patients who do not accept their participation in this clinical trial.
•- Patients who do not have legal capacity.
•- Morbid obesity (BMI > 35 kg / m2 in women and > 42 kg / m2 in men).
•- Basal values ??of systolic blood pressure = 95 mmHg or a heart rate = 60x ' .
•-Disorders of conduct or anxiety-depressive syndrome.
•- Treatment with chronic psychotropic drugs or opiates.
•- Pregnancy
•- Background Of alcohol abuse .
•- Documented allergy to morphic drugs , paracetamol, metamizol and dexketoprofen.
•- Visual secondary alterations to neurological pathologies, retinopatía diabetic and surgery or anomalies of the iris.
•- Neurological impairment at the level of the midbrain.

发起方

Fundació Hospital Vall Hebron Institut de Recerca