NCT07329829

Brief Summary

This study is designed to find the best way to control pain after hip surgery performed through a side (lateral) incision. Two different types of nerve blocks used before the operation will be compared. In one group, patients will receive a Pericapsular Nerve Group (PENG) block, which numbs the main nerves that carry pain signals from the hip joint. In the other group, patients will receive a PENG block together with a Lateral Femoral Cutaneous Nerve (LFCN) block, which adds extra pain relief for the skin and outer part of the thigh. A total of 72 patients between 18 and 80 years old will take part in this study. All operations will be done under spinal anesthesia. Pain levels will be measured several times during the first 24 hours after surgery using a simple 0-10 pain scale. Patients will receive pain medicine through a pump that allows them to press a button when they feel pain. The total amount of medicine used will be recorded. The researchers will also monitor when patients first need pain medicine, when they can start walking, how satisfied they are with pain control, and if they experience side effects such as nausea or dizziness. By comparing the two methods, the study aims to see whether adding the LFCN block to the PENG block provides better pain control, lower drug use, faster recovery, and higher patient comfort after hip surgery.

Trial Health

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
72

participants targeted

Target at P50-P75 for not_applicable

Timeline
0mo left

Started Nov 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress94%
Nov 2025Jul 2026

Study Start

First participant enrolled

November 1, 2025

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

December 27, 2025

Completed
13 days until next milestone

First Posted

Study publicly available on registry

January 9, 2026

Completed
23 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2026

Completed
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2026

Expected
Last Updated

January 12, 2026

Status Verified

July 1, 2025

Enrollment Period

3 months

First QC Date

December 27, 2025

Last Update Submit

January 9, 2026

Conditions

Keywords

Pericapsular Nerve Group Block (PENG Block)Lateral Femoral Cutaneous Nerve Block (LFCN Block)Hip SurgeryRegional AnesthesiaPostoperative AnalgesiaPain ControlOpioid ConsumptionEarly Mobilization

Outcome Measures

Primary Outcomes (1)

  • Postoperative Pain Intensity (NRS Score)

    Postoperative pain intensity will be assessed using the Numeric Rating Scale (NRS), ranging from 0 (no pain) to 10 (worst imaginable pain), both at rest and during movement.

    2, 6, 12, and 24 hours postoperatively

Secondary Outcomes (3)

  • Total Postoperative Opioid Consumption

    First 24 hours postoperatively

  • Patient Satisfaction Score

    Within the first 24 hours postoperatively

  • Time to First Mobilization

    Within the first 24 hours postoperatively

Study Arms (2)

PENG BLOCK GROUP

EXPERIMENTAL

An ultrasound-guided Pericapsular Nerve Group (PENG) block will be performed preoperatively using standard local anesthetic techniques to provide postoperative analgesia in patients undergoing lateral incision hip surgery.

Procedure: Pericapsular nerve group (PENG) block

PENG + LFCN BLOCK GROUP

EXPERIMENTAL

Patients in this group will receive a preoperative ultrasound-guided Pericapsular Nerve Group (PENG) block combined with a Lateral Femoral Cutaneous Nerve (LFCN) block for postoperative analgesia prior to lateral incision hip surgery under spinal anesthesia.

Procedure: Pericapsular nerve group (PENG) blockProcedure: Lateral Femoral Cutaneous Nerve (LFCN) Block

Interventions

An ultrasound-guided Lateral Femoral Cutaneous Nerve (LFCN) block will be performed preoperatively as an adjunct to the PENG block to enhance postoperative analgesia in patients undergoing lateral incision hip surgery.

PENG + LFCN BLOCK GROUP

An ultrasound-guided Pericapsular Nerve Group (PENG) block will be performed preoperatively using standard local anesthetic techniques to provide postoperative analgesia in patients undergoing lateral incision hip surgery.

PENG + LFCN BLOCK GROUPPENG BLOCK GROUP

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Patients aged between 18 and 80 years
  • Patients scheduled for elective or trauma-related hip surgery performed through a lateral incision under spinal anesthesia
  • Patients receiving a preoperative ultrasound-guided Pericapsular Nerve Group (PENG) block or a PENG block combined with a Lateral Femoral Cutaneous Nerve (LFCN) block
  • American Society of Anesthesiologists (ASA) physical status I-III
  • Patients with full orientation and the ability to cooperate
  • Ability to understand the study procedures and provide written informed consent

You may not qualify if:

  • Contraindications to regional anesthesia, including coagulopathy or local infection at the injection site
  • Presence of neuropathic disorders or conditions that may affect pain perception, including chronic analgesic use
  • Requirement for conversion to general anesthesia
  • Postoperative admission to the intensive care unit
  • Known allergy or hypersensitivity to opioids or local anesthetics
  • American Society of Anesthesiologists (ASA) physical status IV-V

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Basaksehir Çam and Sakura City Hospital

Istanbul, BASAKSEHİR, 34490, Turkey (Türkiye)

Location

Related Publications (4)

  • Roy R, Agarwal G, Pradhan C, Kuanar D. Total postoperative analgesia for hip surgeries, PENG block with LFCN block. Reg Anesth Pain Med. 2019 Mar 28:rapm-2019-100454. doi: 10.1136/rapm-2019-100454. Online ahead of print. No abstract available.

    PMID: 30923252BACKGROUND
  • Yoo SH, Lee MJ, Beak MH, Kim WJ. Efficacy of Supplemental Ultrasound-Guided Pericapsular Nerve Group (PENG) Block Combined with Lateral Femoral Cutaneous Nerve Block in Patients Receiving Local Infiltration Analgesia after Hip Fracture Surgery: A Prospective Randomized Controlled Trial. Medicina (Kaunas). 2024 Feb 12;60(2):315. doi: 10.3390/medicina60020315.

    PMID: 38399602BACKGROUND
  • Pascarella G, Costa F, Strumia A, Ruggiero A, Remore LM, Lanteri T, Hazboun A, Longo F, Gargano F, Schiavoni L, Mattei A, Agro FE, Carassiti M, Cataldo R. Lateral Femoral Cutaneous Nerve Block or Wound Infiltration Combined with Pericapsular Nerve Group (PENG) Block for Postoperative Analgesia following Total Hip Arthroplasty through Posterior Approach: A Randomized Controlled Trial. J Clin Med. 2024 May 2;13(9):2674. doi: 10.3390/jcm13092674.

    PMID: 38731203BACKGROUND
  • Liang L, Zhang C, Dai W, He K. Comparison between pericapsular nerve group (PENG) block with lateral femoral cutaneous nerve block and supra-inguinal fascia iliaca compartment block (S-FICB) for total hip arthroplasty: a randomized controlled trial. J Anesth. 2023 Aug;37(4):503-510. doi: 10.1007/s00540-023-03192-6. Epub 2023 Apr 12.

    PMID: 37043081BACKGROUND

MeSH Terms

Conditions

Hip FracturesAgnosia

Interventions

Dental Occlusion

Condition Hierarchy (Ancestors)

Femoral FracturesFractures, BoneWounds and InjuriesHip InjuriesLeg InjuriesPerceptual DisordersNeurobehavioral ManifestationsNeurologic ManifestationsNervous System DiseasesSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

DentistryDental Physiological PhenomenaDigestive System and Oral Physiological Phenomena

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER GOV
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
ASSOCIATE PROFESSOR

Study Record Dates

First Submitted

December 27, 2025

First Posted

January 9, 2026

Study Start

November 1, 2025

Primary Completion

February 1, 2026

Study Completion (Estimated)

July 1, 2026

Last Updated

January 12, 2026

Record last verified: 2025-07

Locations