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Non-guided hip injections are a safe and accurate method of treatment for patients undergoing hip arthroscopy due to Femeroacetabular Impingement (FAI)

To evaluate the efficacy of the anterior approach for blind intra-articular hip injections in patients undergoing hip arthroscopy due to Femoroacetabular Impingement (FAI)

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12612000873820
Enrollment
40
Registered
2012-08-17
Start date
2012-04-05
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

Lately, a new method for intraarticular hip injection has been increasingly considered, and is believed to be very accurate, eliminating the need for imaging assistance (which enables the surgeon to apply the treatment in an outpatient environment). This blind method of injection will be assessed by: 1. Injecting small amount of air into the hip prior to hip arthroscopy surgery in the operating theatre, in the same technique as it is performed on a regular basis, but via a different approach (anterior versus lateral) and initially with no image assistance. The location of the needle will then be assessed using fluoroscopy. 2. Injecting small amount of Methylene Blue into the hip prior to total hip replacement surgery, verifying its location and injection accuracy later during the same operation. Our hypothesis is that anterior hip injection technique, without imaging guidance, would yield high accuracy rates. Hip injections able to be performed without imaging will also lead to less expense for the patient and community with a reduction in burden on imaging services.

Interventions

Treatment group will have a 19G spinal needle inserted into the anterior hip joint and followed by an air arthrogram (10ml of air inserted through needle). This air will enable the braking of the suction seal of the joint to enable traction, without which the surgery cannot commence. The position of the needle would then be verified by fluoroscopy. This process will take approximately 3-4 minutes and will be immediately followed by the commencement of the patient's scheduled hip arthroscopy s

Treatment group will have a 19G spinal needle inserted into the anterior hip joint and followed by an air arthrogram (10ml of air inserted through needle). This air will enable the braking of the suction seal of the joint to enable traction, without which the surgery cannot commence. The position of the needle would then be verified by fluoroscopy. This process will take approximately 3-4 minutes and will be immediately followed by the commencement of the patient's scheduled hip arthroscopy surgery.

Sponsors

Dr David Young
Lead SponsorIndividual

Study design

Allocation
Non-randomised trial
Intervention model
Single group
Primary purpose
Treatment

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

Male or female patients aged between 18-50 healthy patients undergoing hip arthroscopy due to FAI No previous total hip replacement surgery

Exclusion criteria

a) Patients with relative or proven dysplastic hip joints determined by CE angle and/or extreme version abnormalities as measured on apical CT/MR cuts and pelvic XR. b) patients with an artificial joint (Total hip replacement)

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026