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Combined Ultrasound and Fluoroscopy-guided Technique for Anterior Hip Denervation

Combined Ultrasound and Fluoroscopy-guided Technique for Treatment of Hip Pain. A Pilot Study for a Suggested Approach for Anterior Hip Denervation

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04945668
Enrollment
16
Registered
2021-06-30
Start date
2021-07-31
Completion date
2021-10-31
Last updated
2021-06-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hip Fractures

Brief summary

Hip fracture is a challenging geriatric problem for health care professionals, especially in patients with multiple comorbidities. In patients with inoperable hip fractures secondary to severe comorbid conditions, the pain can lead to significant challenges in nursing care. A recent anatomical study confirmed the innervation of the anterior hip by these 3 main nerves but also found that the AON and FN play a greater role in the anterior hip innervation than previously reported.

Detailed description

The aim of this study is to help to target a suggested optimum landmark and determine the volume of injectate that can cover the distribution of the anterior articular branches supplying the hip joint. The anterior hip capsule is innervated by the ON, accessory obturator nerve (AON), and FN as reported by previous anatomic studies. The anterior capsule is the most richly innervated section of the joint. Ultrasound-guided technique for blockade of these articular branches to the hip, the PENG (Pericapsular Nerve Group) block reported significantly reduced pain scores compared with baseline. With the current understanding of the complex innervations of the hip joint, it is difficult to provide complete effective radiofrequency ablation to the articular branches supplying the hip joint. Chemical hip denervation using ultrasound was reported by previous case reports or series without mentioning a well-defined target point or an optimum injectate volume.

Interventions

PROCEDUREModified technique for pericapsular nerve group block

with the patient in the supine position, ultrasound probe in a transverse plane over the anterior inferior iliac spine (AIIS) and then aligned with the pubic ramus. In this view, the ilio pubic eminence (IPE), the iliopsoas muscle and tendon will be observed. A spinal needle will be inserted from lateral to medial in an in-plane approach to place the tip between the psoas tendon and the pubic ramus. Fluoroscopic image will be taken to confirm the needle tip position in the target site. Following negative aspiration, 15 ml dye will be injected in 5-mL increments while observing for adequate spread using fluoroscopy followed by 15ml local anesthetic

Sponsors

Mansoura University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
50 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* ASA physical status I, II, and III. * Patients scheduled for elective or emergent hip fractures.

Exclusion criteria

* Patient refusal. * Neuromuscular diseases (as myopathies, myasthenia gravies…) * Hematological diseases, bleeding, or coagulation abnormality. * Psychiatric diseases. * Local skin infection and sepsis at the site of the block. * Known intolerance to the study drugs. * Body Mass Index \> 40 Kg/m2. * Multiple trauma patients.

Design outcomes

Primary

MeasureTime frameDescription
The success rate to target a suggested optimal landmarkjust after skin punctureIs defined as the percentage of success to reach the target point for injection with needle punctures to up to 4 skin punctures.

Secondary

MeasureTime frameDescription
The number of skin punctures:just after skin puncture for the blockIs defined as the total number of skin punctures for either getting the target point or not.
the total number of needle passes required for obtaining the target landmarkjust after skin punctureIs defined as the total number of forward advancements of the spinal needle i.e. withdrawal and redirection without exiting the skin (sum of passes of all punctures).
The optimum volume of the injectate30 minutes before surgery.Is defined as the optimum volume of the injectate to cover the target innervation area.
Pain measurement at restPrior to performing of nerve block, 15, 30 minutes after block performance10-cm visual analog scale (VAS) for pain, where 0 is equal to no pain and 10 indicates the worst possible pain.
Success rate of first skin puncturejust after skin punctureIs defined as the number of getting the target point from the first skin puncture
Incidence of block failed block30 minutes after Local Anesthetic injectionIs defined as less than 50% pain relief of pain i.e. (less than 50% of VAS score is reduced after the block
Time for first analgesic requestWithin 24 hours after surgerythe time passed from LA injection to the patient need of first analgesia
Patient satisfaction scoreWithin 24 hours after the nerve blockFrom zero=Poor, 1=fair, 2=good, 3=very good to 5=excellent
Complications:Within 24 hours after the nerve blockpresence or absence of unintentional vascular puncture, hematoma formation, parasthesia
Pain measurement on movement (attempted hip flexion to 15 degrees):Prior to performing of nerve block, 15, 30 minutes after block performance10-cm visual analog scale (VAS) for pain, where 0 is equal to no pain and 10 indicates the worst possible pain,

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026