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The Effect of Two Different Analgesic Techniques on Postoperative Recovery Quality

RecruitingNAAges 18 Years - 65 YearsFemaleAtaturk University
NCT06766994 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

Hysterectomy is one of the most frequently performed surgical procedures after Caesarean section in many countries of the world and involves the removal of the uterine corpus with or without the cervix (total hysterectomy) or without the cervix (subtotal or supracervical hysterectomy) to treat a range of gynecological problems. Hysterectomy is performed abdominally, vaginally with laparotomy, or using minimally invasive techniques (laparoscopy, robotic surgery). The abdominal route for hysterectomy is the preferred route in 60-80% of these surgeries. Postoperative recovery is a complex condition affected by various factors such as patient characteristics, surgical procedure, and anesthesia. There are many tools available to measure recovery quality. In recent years, the concept of recovery quality perceived by the patient has attracted attention. The Quality of Recovery-40 questionnaire

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📋 Eligibility rules (as published)
Inclusion Criteria: * Patients scheduled to undergo abdominal hysterectomy surgery under general anesthesia * Ages between 18-65 * American Society of Anesthesiologists classification I-II Exclusion Criteria: * Patients with a BMI ≥ 35, * Patients with allergies to the drugs to be used in the study, * Patients with severe liver or kidney failure, * Patients with a history of long-term use of nonsteroidal anti-inflammatory and opioid analgesics, * Patients with a history of gastrointestinal bleeding, peptic ulcers or inflammatory bowel disease, * Patients with a history of diabetes or other neuropathic diseases, * Patients who developed atrioventricular block and bradycardia before surgery, * Patients with a history of serious underlying respiratory disease and psychiatric diseases, * Patients with ASA stage 3 or higher, * Patients who cannot use a patient-controlled analgesia (PCA) device, * Patients who need to stop the drug used in the study during surgery for any reason, * Patients who do not consent to participate in the study
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What it tests

  • intrathecal morphine
  • Erector Spinae Plane Block
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Where

1 site
Ataturk University
Erzurum, Turkey (Türkiye)
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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