Doxycycline Treatment in Graves' Orbitopathy
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Purpose
The aim of this study is to evaluate the effects of subantimicrobial dose doxycycline (50 mg/d), administered three months, for patients with active moderate-severe Graves' Orbitopathy (GO).
| Condition | Intervention | Phase |
|---|---|---|
|
Graves Ophthalmopathy Graves Disease Eye Diseases Thyroid Diseases Endocrine System Diseases Eye Diseases, Hereditary Hyperthyroidism Autoimmune Diseases Immune System Diseases |
Drug: Doxycycline |
Phase 1 Phase 2 |
| Study Type: | Interventional |
| Study Design: | Endpoint Classification: Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | The Effect of Subantimicrobial Dose Doxycycline in Graves' Orbitopathy |
- • European Group on Graves' Orbitopathy (EUGOGO) Clinical Activity Score [ Time Frame: 3 months ] [ Designated as safety issue: No ]Clinical Activity Score is a validated index of Graves' orbitopathy that assigns one point to the presence of: 1.spontaneous retrobulbar pain, 2. pain on up/downgaze, 3. redness of eyelids, 4. redness of conjunctiva, 5. swelling of eyelids, 6. inflammation of caruncle/plica, 7. chemosis. The maximal clinical activity score (CAS) is thus 7.
- • Health related quality of life questionnaires (GO-QoL) [ Time Frame: 3 months ] [ Designated as safety issue: No ]
- • Safety and tolerability as assessed by adverse events, vital signs [ Time Frame: 6 months. ] [ Designated as safety issue: Yes ]
- Relapse [ Time Frame: 6 months ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 14 |
| Study Start Date: | October 2012 |
| Estimated Study Completion Date: | October 2013 |
| Estimated Primary Completion Date: | October 2013 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: Doxycycline
Tablets Doxycycline 50 mg PO per day for three months
|
Drug: Doxycycline
Tab. Doxycycline 50 mg PO per day for 3 months
Other Names:
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Detailed Description:
Graves'orbitopathy is an autoimmune disease characterised by an inflammatory phase followed by fibrosis. Surgery to correct eyelid swelling, proptosis, and diplopia is effective, but can not be done until the inflammatory phase has passed. To arrest the inflammatory phase, several types of immunosuppressive treatments have been investigated. Corticosteroids are the first-choice immunosuppressive treatment, but they often cause severe side-effects.
Subantimicrobial dose doxycycline posses known anti-inflammatory effects that are separate from their antibacterial mode of action. This mode of action has lead to the routine use of subantimicrobial dose doxycycline for rosacea, periodontitis and multiple sclerosis.
We propose to test the effect of subantimicrobial dose doxycycline for non-sight threatening, moderate-severe, inflammatory GO.
Eligibility| Ages Eligible for Study: | 18 Years to 65 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Clinical diagnosis of Graves' Orbitopathy
- Moderate-severe GO According to EUGOGO statements, patients with moderate-severe GO usually have any one or more of the following:lid retraction≥2mm, moderate or severe soft tissue involvement, exophthalmos≥3mm above normal for race and gender, inconstant, or constant diplopia.
- Clinical activity score ≥ 3
- Being euthyroid for at least 2 months before the date of inclusion
- Must be able to swallow tablets
- Written informed consent is obtained
Exclusion Criteria:
- Mild Graves' Orbitopathy
- Sight-threatening Graves' Orbitopathy
- Clinical activity score < 3
- Previous treatment for GO Oral steroids, intravenous steroids, radiotherapy
- Pregnant females as determined by positive (serum or urine) Human chorionic gonadotropin (hCG) test at screening or prior to dosing, or lactating females
- Uncontrolled diabetes or hypertension
- History of mental / psychiatric disorder
- Hepatic dysfunction (Albumin (Alb),Aspartate Transaminase (AST), Alanine Aminotransferase (ALT) and Alkaline phosphates levels must be within normal range for eligibility)
- Renal impairment (Urea and Creatinine levels must be within normal range)
- Doxycycline allergy or intolerance
Contacts and Locations| Contact: Dan Liang, MD | 0086-20-87331766 | linml0754@gmail.com |
| China, Guangdong | |
| Zhongshan Ophthalmic Center | Recruiting |
| Guangzhou, Guangdong, China, 510060 | |
| Contact: Dan Liang, MD 0086-20-87331766 liangd2@mail.sysu.edu.cn | |
| Principal Investigator: Dan Liang, MD | |
| Principal Investigator: | Dan Liang, MD | Zhongsh Ophthalmic Center |
More Information
Additional Information:
No publications provided
| Responsible Party: | Dan Liang, MD, Sun Yat-sen University |
| ClinicalTrials.gov Identifier: | NCT01727973 History of Changes |
| Other Study ID Numbers: | GO-DOXY-1 |
| Study First Received: | November 12, 2012 |
| Last Updated: | May 27, 2013 |
| Health Authority: | China: Ethics Committee |
Keywords provided by Sun Yat-sen University:
|
Graves' orbitopathy Graves´ ophthalmopathy Thyroid eye disease Thyroid-associated ophthalmopathy |
Doxycycline EUGOGO CAS |
Additional relevant MeSH terms:
|
Hyperthyroidism Autoimmune Diseases Endocrine System Diseases Eye Diseases Eye Diseases, Hereditary Graves Disease Genetic Diseases, Inborn Immune System Diseases Thyroid Diseases Graves Ophthalmopathy Exophthalmos |
Orbital Diseases Goiter Doxycycline Doxycycline hyclate Anti-Bacterial Agents Anti-Infective Agents Therapeutic Uses Pharmacologic Actions Antimalarials Antiprotozoal Agents Antiparasitic Agents |
ClinicalTrials.gov processed this record on June 17, 2013