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Evaluation of Post-operative Pain Management Methods in Patients Undergoing Total Hip Arthroplasty.

Status: Recruiting
Location: See location...
Intervention Type: Procedure, Drug
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Pain after hip replacement surgery is often severe and is commonly treated with opioids, which may cause nausea, vomiting, sedation, difficulty passing urine and slow breathing. This study will compare two ways of controlling pain in adults having hip surgery under spinal anesthesia. One group will receive morphine added to the spinal injection. The other group will receive an ultrasound-guided pericapsular nerve group (PENG) block, in which local anesthetic is injected near the nerves that carry pain signals from the hip joint. Participants will be assigned to one of the two groups by chance. Sixty-four adults aged 18 to 65 years will take part, with 32 in each group. Pain scores at rest and during movement, the total amount of morphine used through a patient-controlled pump, the time until the first request for extra pain medicine, the amount of additional paracetamol used, side effects such as nausea and vomiting, and complications related to the block will be compared between the groups during the first 48 hours after surgery.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• Age 18 to 65 years

• American Society of Anesthesiologists physical status I, II or III

• Scheduled for unilateral hip surgery under spinal anesthesia, including hip fracture surgery and hip replacement surgery

• Able to understand and use the Visual Analog Scale and the patient-controlled analgesia device

• Written informed consent

Locations
Other Locations
Turkey
Selcuk University Hospital
RECRUITING
Konya
Contact Information
Primary
NARGIZ MAMMADOVA
dr.nergiz93@gmail.com
+90 552 886 23 56
Backup
Inci KARA
drincikara@yahoo.com
+90 505 483 18 19
Time Frame
Start Date: 2026-08-24
Estimated Completion Date: 2026-09-25
Participants
Target number of participants: 64
Treatments
Active_comparator: Intrathecal Morphine Group
Patients receive spinal anesthesia with 10 mg hyperbaric bupivacaine 0.5% plus 100 micrograms of preservative-free morphine into the intrathecal space.
Experimental: PENG Block Group
Patients receive spinal anesthesia with 10 mg hyperbaric bupivacaine 0.5% alone, followed by an ultrasound-guided pericapsular nerve group (PENG) block on the operated side with 20 mL of 0.5% bupivacaine.
Related Therapeutic Areas
Sponsors
Leads: Selcuk University

This content was sourced from clinicaltrials.gov