UmraniyeERH
Istanbul, Umraniye, 34734, Turkey (Türkiye)
Location status: Recruiting
NCT Number: NCT06183528
The hypothesis of this study is that patients who undergo PENG block in before Total Hip Artroplasthy (THA) surgery with spinal anesthesia will have reduced postoperative pain scores, less need for opioid analgesics and earlier mobilisation.
Interested in participating?
Request Info40 year–85 year
All sexes
Interventional
Not applicable
Istanbul, Umraniye, 34734, Turkey (Türkiye)
Location status: Recruiting
This prospective randomised controlled study included a total of 60 patients aged 40-85 years who underwent THA surgery under spinal anaesthesia. Patients were divided into two groups as PENG block (n:30) and non-PENG block (n:30). PENG block was placed in the fascial plane between the pseudotendon and pubic ramus with USG in-plane technique, 20 ml of 0.5% bupivacaine was administered and surgery was initiated. The primary outcome of the study was to investigate the effect of preoperative PENG block application on postoperative pain, opioid requirement, mobilisation time, hip joint patency and length of hospital stay in patients undergoing THA surgery. The secondary outcome was to investigate the effect of PENG block on perioperative haemodynamics and postoperative side effects.
For multimodal analgesia, 10 ml 0.5% bupivacaine + 10 ml 2% lidocaine is infiltrated into the surgical wound incision line by the surgical team at the end of surgery. After tramadol 50 mg loading with PCA device, a basal rate of 5-10 mg/hour (20 mg bolus dose + 30 minutes lock time) is given with paracetamol 10 mg/kg iv (8 hours interval).
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Under 40 years of age, over 85 years of age,
With ultrasonography-guided PENG block, the femoral, obturator and accessory obturator nerve branches that provide sensory innervation of the anterior surface of the hip joint capsule are blocked .
Time frame: recovery room 30 min, 12., 24. and 48. hours in the postoperative period
VAS pain score
Time frame: 24 -48 hours
walking 5 steps with walker
Time frame: 24. hours
Measurement of joint movement angle with goniometer (angle)
Time frame: 48 hours
Tramadol total usage (mg)
Time frame: The first 48 hours after performing the PENG block
motor block, nausea, vomiting, anaphylaxis, nerve damage
Time frame: T1: 30 minutes (min) after spinal anesthesia, T2: at the end of the surgical procedure, T3: at 30 minutes after recovery
heart rate, mean arterial pressure
Time frame: day
hospitalization and discharge time for surgery
Contact information is provided by the study sponsor or research team.
hale arkan tuna, specialist dr
CONTACT
zeliha tuncel, ass prof
CONTACT
Umraniye Education and Research Hospital
Other Gov
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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