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NCT06821516
Comparison of Pain Relief Methods for Hip Surgery: A Study on Two Different Nerve Block Techniques
NA trial testing Evaluation of the postoperative analgesic effectiveness of PENG block in participants undergoing total hip arthroplasty under spinal anesthesia in Opioid Consumption, Postoperative in 52 participants. Currently enrolling.
1 March 2026
Quick facts
| Lead sponsor | Başakşehir Çam & Sakura City Hospital |
|---|---|
| Phase | NA |
| Status | Recruiting now |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | double |
| Primary purpose | prevention |
| Enrollment | 52 |
| Start date | 21 January 2025 |
| Primary completion | 1 March 2026 |
| Estimated completion | 1 June 2026 |
| Sites | 1 location across Turkey (Türkiye) |
Drugs / interventions tested
- Evaluation of the postoperative analgesic effectiveness of PENG block in participants undergoing total hip arthroplasty under spinal anesthesia
- Evaluation of the postoperative analgesic effectiveness of lumbar erector spinae block in participants undergoing total hip arthroplasty under spinal anesthesia
Conditions studied
- Opioid Consumption, Postoperative — all drugs for Opioid Consumption, Postoperative →
- Pain, Postoperative — all drugs for Pain, Postoperative →
- Nerve Block — all drugs for Nerve Block →
- PENG Block — all drugs for PENG Block →
Sponsor
Başakşehir Çam & Sakura City Hospital
Who can join
18 and older, any sex, with Opioid Consumption, Postoperative or Pain, Postoperative. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This prospective randomized comparative study aims to compare the analgesic efficacy of pericapsular nerve group block (PENG) and lumbar erector spinae plane block (L-ESP) groups to relieve postoperative pain in participants over the age of 18 undergoing total hip arthroplasty under spinal anesthesia. The main question it aims to answer is: To demonstrate whether PENG block or L-ESP block is more effective in postoperative analgesia in patients undergoing total hip arthroplasty surgery based on pain scores, opioid consumption, and patient satisfaction. Total hip arthroplasties cause severe pain with movement in the postoperative period. After surgery, the movements of the participants are severely restricted, which increases the possibility of complications. In this study, the participants' pain status, VAS score, opioid consumption through patient-controlled analgesia, and patient satisfaction will be measured with a questionnaire for 24 hours at predetermined time points and then compared. Both types of blocks have pain-relieving effects. This study will only investigate which one is more effective in reducing pain, and there will be no deficiency in relieving the pain of the participants.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT06821516
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
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Related trials
Other recruiting trials for Opioid Consumption, Postoperative
Currently open trials in the same condition.
- NCT07427043 — Robotic Opioid-free Prostatectomy Enhanced Strategy (ROPES) · Phase 3 · recruiting
- NCT07226700 — Suzetrigine in Total Hip Arthroplasty · Phase 3 · recruiting
- NCT07403734 — Evaluation of the Postoperative Efficacy of Bilateral Lumbar Erector Spinae Plane Block (ESPB) in Patients Undergoing Lu · active not recruiting
Other Başakşehir Çam & Sakura City Hospital trials
Trials by the same sponsor.
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- NCT07199049 — Neuro-Mimic Indicators of Anesthesia Depth During General Anesthesia · not yet recruiting
- NCT07194707 — Effect of Operating Room Noise on BIS and Hemodynamics Under General Anesthesia · not yet recruiting
- NCT07327125 — Effect of Skin Closure Techniques on Body Image in Women Undergoing Gynecologic Surgery · NA · recruiting
- NCT07453641 — White Noise and Crying Duration After Invasive Procedures in Infants · NA · recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06821516 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Başakşehir Çam & Sakura City Hospital
- Last refreshed: 12 February 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06821516.
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