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New Treatment for Patients With Temporal Hollowing After Lateral Wall Decompression

Not Applicable
Completed
Conditions
Thyroid-Associated Ophthalmopathy
Interventions
Procedure: Autologous fat injection
Procedure: Hyaluronic acid injection
Registration Number
NCT02693808
Lead Sponsor
Haukeland University Hospital
Brief Summary

The purpose of this study is to determine whether injection of autologous fat or hyaluronic-acid injections in temporal region are effective in the treatment of temporal hollowing after lateral wall decompression in patients with thyroid eye disease.

Detailed Description

Grave's disease is one of the most common autoimmune diseases. Thyroid eye disease is affecting nearly 50% of patients with Grave's disease. Surgical treatment may address several of the manifestations, including the increased volume of the orbital contents. Decompression of the orbit can be achieved by removing the lateral orbital walls; "lateral wall decompression".

In a retrospective study at the Department of Ophthalmology, Haukeland University Hospital, about half of the patients had a disfiguring hollowing in the temporal region after lateral wall decompression. The patient reported outcome of the procedure is clearly an indication for further esthetic treatment. However, until now the treatment option for these patients have been limited, or simply neglected. The investigators have contacted over 40 patients with this complication that want treatment.

In this project the investigators will treat bilateral hollowing with injection of autologous fat in one temporal region and hyaluronic-acid injections on the opposite side. Participants with unilateral hollowing will be randomized to one of the treatment options. Outcomes will be evaluated by clinical examination, photographs and ultrasound volume measurement at 6, 12, 18 and 24 months postoperatively. The participants will be retreated at these follow up intervals if necessary.

The project will be an interventional, prospective follow-up study and is approved by the regional ethics committee. The study will be the first of its kind to date as the investigators will be able to prospectively evaluate the effect of autologous fat injections to hyaluronic-acid injections in the same patient for the same condition.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
29
Inclusion Criteria
  • Disfiguring temporal hollowing after lateral wall decompression.
  • The participant want treatment for temporal hollowing

Exclusion Critera:

  • The participant dont want treatment for temporal hollowing
Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Autologous fat injectionHyaluronic acid injectionPatients have undergone lateral orbital wall decompression on both sides. Temporal hollowing after surgery will be treated with injection on one side with autologous fat and the other side with long-lasting hyaluronic acid.
Hyaluronic acid injectionAutologous fat injectionPatients have undergone lateral orbital wall decompression on both sides. Temporal hollowing after surgery will be treated with injection on one side with autologous fat and the other side with long-lasting hyaluronic acid.
Autologous fat injectionAutologous fat injectionPatients have undergone lateral orbital wall decompression on both sides. Temporal hollowing after surgery will be treated with injection on one side with autologous fat and the other side with long-lasting hyaluronic acid.
Hyaluronic acid injectionHyaluronic acid injectionPatients have undergone lateral orbital wall decompression on both sides. Temporal hollowing after surgery will be treated with injection on one side with autologous fat and the other side with long-lasting hyaluronic acid.
Primary Outcome Measures
NameTimeMethod
Number of patients with satisfactory objective cosmetic and functional outcome2 years

Evaluation of photographs (1 to 3/Normalized to disfiguring)

Secondary Outcome Measures
NameTimeMethod
Number of reinjections2 years

Number.

Number of patients with satisfactory subjective cosmetic and functional2 years

Patient reported perception of outcome (1 to 3/Normalized to disfiguring)

Volume of injected substance measured by ultrasonography2 years

ml

Number and type of complications2 years

Hematoma, infection, embolization.

Trial Locations

Locations (1)

Department of Ophthalmology Haukeland University Hospital

🇳🇴

Bergen, Hordaland, Norway

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