Actively Recruiting
Combined Acupressure Effects on Post-Thoracotomy Pain and Lung Volume
Led by Özgül Aydemir · Updated on 2026-02-13
80
Participants Needed
1
Research Sites
104 weeks
Total Duration
On this page
Sponsors
Ö
Özgül Aydemir
Lead Sponsor
I
Istanbul University - Cerrahpasa
Collaborating Sponsor
AI-Summary
What this Trial Is About
Pain is a subjective, sensory and emotionally unpleasant experience resulting from real or hidden injuries in tissues. The pain experience is a subjective and unique experience in physiological and psychological terms and is the first negative sensory experience of the patient after the surgical procedure. Thoracotomy is an invasive surgical incision that causes severe postoperative pain due to the negative effect on the ribs, muscles and peripheral nerves. During thoracic surgery, anatomical lung resection is performed through posterolateral thoracotomy. Surgical incision during thoracotomy surgery is the most severe cause of postoperative pain. Epidural analgesia, peripheral nerve block and systematic treatment methods are used in post-thoracotomy pain management. Opioid use is frequently preferred in post-thoracotomy pain management. Although thoracotomy pain can mostly be controlled with opioid analgesics, excessive use of opioids may lead to respiratory suppression, constipation, suppression of cough, nausea, vomiting and many other possible side effects. Ineffective postoperative pain management may lead to postoperative complications such as increased cardiac workload, prolonged pulmonary rehabilitation and delayed wound healing. The use of holistic non-drug pain relief methods is vital in reducing the need for opioid analgesics and the risk of possible side effects in early postoperative pain management.
CONDITIONS
Official Title
Combined Acupressure Effects on Post-Thoracotomy Pain and Lung Volume
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Underwent thoracotomy
- Undergoing thoracic surgery for the first time
- Classified as ASA (American Society of Anesthesiology) physical status I, II and III
- Presence of a drain upon admission to the intensive care unit
- Conscious, oriented, and cooperative
- Provided verbal and written informed consent after receiving information about the study
You will not qualify if you...
- Intubated
- Persistent anxiety before the surgery
- Diagnosed with panic disorder
- Chemotherapy within the last 6 months
- Diagnosed psychiatric illness or mental health problems
- Presence of edema
- Intraoperative or postoperative complications
- Non-Turkish speaking or presence of hearing or visual impairment
- Body mass index (BMI) greater than 30
- Participation in another clinical trial during the study period
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Özgül Aydemir
Istanbul, Turkey (Türkiye), 34067
Actively Recruiting
Research Team
Ö
Özgül Aydemir, Doctor
CONTACT
Ö
Öykü Kara, Specialist
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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