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Intraorbital Injection Versus Oral Steroid in Anterior Idiopathic Orbital Inflammation

Primary Purpose

Orbital Pseudotumor

Status
Recruiting
Phase
Phase 3
Locations
Iran, Islamic Republic of
Study Type
Interventional
Intervention
Prednisolone
Triamcinolone + Betamethason
Sponsored by
Iran University of Medical Sciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Orbital Pseudotumor

Eligibility Criteria

15 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Dacryoadenitis based on clinical findings and/or imaging with and without adjacent recti muscle myositis

Exclusion Criteria:

  • Abnormal thyroid-stimulating hormone
  • Systemic Vasculitides
  • Bilateral Orbital Inflammation
  • Collagen Vascular Diseases
  • One Seeing Eye
  • Glaucoma
  • Diabetes Mellitus

Sites / Locations

  • Iran University of Medical SciencesRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Intraorbital injection of steroid

Oral Steroid

Arm Description

2 mL of steroid will be ready for each injection session: 1 mL Triamcinolone (40 mg) + 1 mL Betamethasone (6 mg) = 2 mL For Dacryoadenitis without myositis , 1 mL of this compound will be injected at lacrimal gland through 1 site of injection. For Dacryoadenitis plus 1 rectus muscles myositis 1 mL of this compound will be injected at lacrimal gland and 0.5 mL of this compound will be injected at the rectus muscle through 2 separate sites of injection. For Dacryoadenitis plus 2 rectus muscles myositis 1 mL of this compound will be injected at lacrimal gland and 0.5 mL of this compound will be injected at either recti muscles through 3 separate sites of injection.

Each patient will receive oral Prednisolone, 1 mg/kg, for 5-7 days, followed by tapered dose in 12 weeks (according to a pre-defined table of oral administration dose). Daily Omeprazole 40mg p.o and daily Calcium Supplement will also be recommended to avoid complications.

Outcomes

Primary Outcome Measures

Recurrence number
frequency of occurrence of clinical condition showing signs of inflammation recurrence, during or after cessation of steroid therapy
Recurrence time
mean time of occurrence of clinical condition showing signs of inflammation recurrence, during or after cessation of steroid therapy
Adverse Effect
Any significant ocular or systemic side effect reported by the patient or found in examination sessions

Secondary Outcome Measures

Full Information

First Posted
May 7, 2019
Last Updated
February 15, 2023
Sponsor
Iran University of Medical Sciences
Collaborators
Tehran University of Medical Sciences, Mashhad University of Medical Sciences, Shahid Beheshti University of Medical Sciences
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1. Study Identification

Unique Protocol Identification Number
NCT03958344
Brief Title
Intraorbital Injection Versus Oral Steroid in Anterior Idiopathic Orbital Inflammation
Official Title
Intraorbital Injection Versus Oral Steroid in Patients With Anterior Idiopathic Orbital Inflammation: A Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
January 1, 2022 (Actual)
Primary Completion Date
June 1, 2024 (Anticipated)
Study Completion Date
June 1, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Iran University of Medical Sciences
Collaborators
Tehran University of Medical Sciences, Mashhad University of Medical Sciences, Shahid Beheshti University of Medical Sciences

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
A multicenter randomised double-arm clinical trial, to compare safety and efficacy of oral versus intralesional injection of steroid in a group of patients suffering from idiopathic orbital inflammation is designed. Outcome measures include number of recurrences, duration of remission, and side effects.
Detailed Description
Expected to be finished in 3 years, patient enrollment includes 59 patient in each arm of the study. Inclusion criteria consist of clinical and/or imaging evidence of dacryoadenitis with or without adjacent rectus muscles (superior and inferior recti) myositis. Patients meeting following conditions will be excluded: Age < 15 years Diabetes mellitus Collagen Vascular Diseases Vasculitides Biopsy of lacrimal gland denoting a specific diagnosis (i.e. the term "idiopathic" does not apply) Glaucoma Patients who have lost one eye Bilateral disease Abnormal thyroid-stimulating hormone Outcome measures include number of recurrences, duration of remission, and side effects. Patient allocation will be based on blocks of 4. Each patient will undergo lacrimal gland biopsy and subsequently will be allocated to one arm of the study according to a predetermined randomization sequence (balanced block of four). Outcome measures will be recorded in 0, 3 and 6 months after patient enrollment. Patients in oral steroid group will receive 1 mg/kg/day of Prednisolone, tapered in 3 months (based on a detailed table). Patients in injection group will receive 1 shot of 1 mL (20 mg Triamcinolone + 3 mg Betamethason) into the lacrimal gland.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Orbital Pseudotumor

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Model Description
Randomized parallel double arm
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intraorbital injection of steroid
Arm Type
Experimental
Arm Description
2 mL of steroid will be ready for each injection session: 1 mL Triamcinolone (40 mg) + 1 mL Betamethasone (6 mg) = 2 mL For Dacryoadenitis without myositis , 1 mL of this compound will be injected at lacrimal gland through 1 site of injection. For Dacryoadenitis plus 1 rectus muscles myositis 1 mL of this compound will be injected at lacrimal gland and 0.5 mL of this compound will be injected at the rectus muscle through 2 separate sites of injection. For Dacryoadenitis plus 2 rectus muscles myositis 1 mL of this compound will be injected at lacrimal gland and 0.5 mL of this compound will be injected at either recti muscles through 3 separate sites of injection.
Arm Title
Oral Steroid
Arm Type
Active Comparator
Arm Description
Each patient will receive oral Prednisolone, 1 mg/kg, for 5-7 days, followed by tapered dose in 12 weeks (according to a pre-defined table of oral administration dose). Daily Omeprazole 40mg p.o and daily Calcium Supplement will also be recommended to avoid complications.
Intervention Type
Drug
Intervention Name(s)
Prednisolone
Other Intervention Name(s)
Oral Prednisolone
Intervention Description
Oral Tablet
Intervention Type
Drug
Intervention Name(s)
Triamcinolone + Betamethason
Other Intervention Name(s)
Injectable Steroid
Intervention Description
A compound long acting and short acting injectable steroid
Primary Outcome Measure Information:
Title
Recurrence number
Description
frequency of occurrence of clinical condition showing signs of inflammation recurrence, during or after cessation of steroid therapy
Time Frame
up to 6 months
Title
Recurrence time
Description
mean time of occurrence of clinical condition showing signs of inflammation recurrence, during or after cessation of steroid therapy
Time Frame
up to 6 months
Title
Adverse Effect
Description
Any significant ocular or systemic side effect reported by the patient or found in examination sessions
Time Frame
up to 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
15 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Dacryoadenitis based on clinical findings and/or imaging with and without adjacent recti muscle myositis Exclusion Criteria: Abnormal thyroid-stimulating hormone Systemic Vasculitides Bilateral Orbital Inflammation Collagen Vascular Diseases One Seeing Eye Glaucoma Diabetes Mellitus
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Mohsen B Kashkouli, MD
Phone
00989121777003
Email
mkashkouli2@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Nasser Karimi, MD
Phone
+989123272376
Email
karimi.na@iums.ac.ir
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mohsen B Kashkouli, MD
Organizational Affiliation
Iran University of Medical Sciences
Official's Role
Principal Investigator
Facility Information:
Facility Name
Iran University of Medical Sciences
City
Tehrān
State/Province
Tehran
Country
Iran, Islamic Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mohsen B Kashkouli, MD
Phone
0098 912 1777003
Email
mkashkouli2@gmail.com

12. IPD Sharing Statement

Citations:
PubMed Identifier
17620331
Citation
Swamy BN, McCluskey P, Nemet A, Crouch R, Martin P, Benger R, Ghabriel R, Wakefield D. Idiopathic orbital inflammatory syndrome: clinical features and treatment outcomes. Br J Ophthalmol. 2007 Dec;91(12):1667-70. doi: 10.1136/bjo.2007.124156. Epub 2007 Jul 9.
Results Reference
background
PubMed Identifier
21349945
Citation
Bijlsma WR, Paridaens D, Kalmann R. Treatment of severe idiopathic orbital inflammation with intravenous methylprednisolone. Br J Ophthalmol. 2011 Aug;95(8):1068-71. doi: 10.1136/bjo.2010.195552. Epub 2011 Feb 24.
Results Reference
background
PubMed Identifier
23839634
Citation
El Nasser A Mohammad A. Local steroid injection for management of different types of acute idiopathic orbital inflammation: an 8-year study. Ophthalmic Plast Reconstr Surg. 2013 Jul-Aug;29(4):286-9. doi: 10.1097/IOP.0b013e318293750c.
Results Reference
result
PubMed Identifier
18071116
Citation
Leibovitch I, Prabhakaran VC, Davis G, Selva D. Intraorbital injection of triamcinolone acetonide in patients with idiopathic orbital inflammation. Arch Ophthalmol. 2007 Dec;125(12):1647-51. doi: 10.1001/archopht.125.12.1647.
Results Reference
result
PubMed Identifier
28872378
Citation
Reggie S, Neimkin M, Holds J. Intralesional corticosteroid injections as treatment for non-infectious orbital inflammation. Orbit. 2018 Feb;37(1):41-47. doi: 10.1080/01676830.2017.1353110. Epub 2017 Sep 5.
Results Reference
result

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Intraorbital Injection Versus Oral Steroid in Anterior Idiopathic Orbital Inflammation

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