Last reviewed · How we verify
NCT06226675
'The Effect of Adding LFCN Block to PENG
NA trial testing PENG Block in Pain, Postoperative in 60 participants. Status unknown.
31 January 2024
Quick facts
| Lead sponsor | Zonguldak Bulent Ecevit University |
|---|---|
| Phase | NA |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | double |
| Primary purpose | prevention |
| Enrollment | 60 |
| Start date | 1 January 2023 |
| Primary completion | 31 January 2024 |
| Estimated completion | 1 April 2024 |
| Sites | 1 location across Turkey (Türkiye) |
Drugs / interventions tested
- PENG Block — full drug profile →
- LFCN block
Conditions studied
- Pain, Postoperative — all drugs for Pain, Postoperative →
- Pain, Acute — all drugs for Pain, Acute →
- Nerve Block — all drugs for Nerve Block →
- Opioid Consumption — all drugs for Opioid Consumption →
Sponsor
Zonguldak Bulent Ecevit University
Who can join
Adults 18 to 75, any sex, with Pain, Postoperative or Pain, Acute. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The incidence of femoral neck fracture in Europe is 330/10000 per year. It is increasing every year due to the aging of the population. In patients 55 years and older, hip fracture-related mortality is estimated to be between 4% and 16% at one month and between 11% and 43% at one year after surgery. The reduced risk of postoperative complications associated with the use of regional anesthesia, shorter mobilization times, and reduced morphine consumption in hip fractures have been reported, and have been incorporated into postoperative pain control as part of multimodal strategies. PENG has been described for postoperative pain control for surgery on the hip joint or for the treatment of post-traumatic pain associated with proximal femur/femoral head fractures. Lateral femoral cutaneous nerve block is used in combination with other peripheral block methods to provide analgesia in the lateral thigh. The investigators aimed to evaluate the effect of adding lateral femoral cutaneous nerve block to PENG block on pain scores and opioid consumption in femoral fracture procedures under spinal anesthesia.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
The effect of adding lateral femoral cutaneous nerve block to pericapsular nerve group (PENG) block in hip surgery on postoperative morphine consumption: A randomized controlled trial.
Şeker DF, Bollucuoğlu K, Baytar Ç, Okyay RD, et al · · 2025 · cited 1× · PMID 40988169 · DOI 10.1097/md.0000000000044588
Verify or expand the search:
- PubMed search for NCT06226675
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of PENG Block
Trials testing the same drug.
- NCT07502248 — PENG Block With or Without PPD Block for Postoperative Analgesia After Total Hip Arthroplasty · NA · not yet recruiting
- NCT07263932 — PENG vs PHPB for Hip Arthroplasty Analgesia · recruiting
- NCT06964282 — Iliopsoas (IPB) and Pericapsular Nerve Group (PENG) Blocks Comparison on Analgesia and Recovery After Total Hip Arthropl · NA · not yet recruiting
- NCT06878963 — COmparison of PENG Block and SIFICB in Hip Fracture Surgeries · NA · not yet recruiting
- NCT06842342 — The Analgesic Effect of Ultrasound-guided Sacral Erector Spinae, Pericapsular Nerve Block and Lumber Plexus Block for Pa · NA · completed
Other recruiting trials for Pain, Postoperative
Currently open trials in the same condition.
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Other Zonguldak Bulent Ecevit University trials
Trials by the same sponsor.
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- NCT07585903 — The Effect of Family-Centered Care Practices In Pediatric Intensive Care Unit · NA · completed
- NCT07382895 — The Relationship Between the ASA Score Determined by Operating Room Nurses and Intubation Duration · completed
- NCT06948383 — SPSIPB vs. SAPB in Breast Surgery · NA · active not 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 NCT06226675 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Zonguldak Bulent Ecevit University
- Last refreshed: 26 January 2024
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/NCT06226675.
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