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A high percentage of patients were dropping out of the study and were not able to complete the protocol.
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The Department of Otolaryngology at Mount Sinai is looking for adults with sinus disease with polyps, otherwise called chronic rhinosinusitis with nasal polyps (CRSwNP). Patients may be eligible to enroll in a study offering a cutting-edge therapy to help reduce symptoms and avoid surgery. The treatment combines an antibiotic (doxycycline) with oral steroids. Oral steroids are the mainstay of medical management for patients with CRSwNP. However, recent studies have shown that doxycycline helps improve symptoms as well by reducing inflammation and killing common bacteria that can cause symptoms. This study is the first to evaluate this combination regimen.
An eligible patient may be treated with either doxycycline and oral steroids OR placebo (sugar pill) and oral steroids for three weeks. Volunteers will participate in the study for to 12 weeks, and will have 4 research visits of 1 hour duration. At each study visit, the patient will under go an endoscopic evaluation and asked to complete a questionnaire describing symptoms. There is no additional cost to be enrolled in the study.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Doxycycline | Experimental | Doxycycline plus oral methylprednisolone and nasal saline sprays |
|
| Sugar pill | Placebo Comparator | placebo pill plus oral methylprednisolone for three weeks. After this, maintenance therapy which includes nasal saline sprays and daily nasal steroid sprays. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Doxycycline | Drug | Doxycycline (200 mg PO X 1 dose on Day 1, then 100 mg PO daily) for Day 2-20 |
|
| Measure | Description | Time Frame |
|---|---|---|
| Sino-nasal Outcome Test (SNOT 22) | a validated 22 item quality of life questionnaire for patients with chronic rhinosinusitis. Range of 0 to 110, higher scores indicate worse outcome | Baseline and 12 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Endoscopic Nasal Polyp Score | 0- Absence of nasal polyps
|
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Inclusion Criteria:
Nasal polyps on nasal endoscopy.
The patient has moderate to severe disease, defined by moderate to severe subjective symptoms (a score greater than 3 on a 10-cm VAS).
The patient is at least 18 years old.
The patient is able to understand and give informed consent.
The patient has clinically diagnosed chronic rhinosinusitis with nasal polyps according to the AAO-HNS diagnostic criteria: At least 2 of the following symptoms/signs:
Exclusion Criteria:
Pregnancy Testing. Women of childbearing potential are required to have a negative serum pregnancy test (with a sensitivity of at least 25 mIU/mL) prior to the first dose of drug. No further pregnancy tests are required since after this visit the patient will no longer be taking tetracycline after 3 weeks.
Women of childbearing potential are defined as follows:
Women are considered not to be of childbearing potential for the following reasons:
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| Name | Affiliation | Role |
|---|---|---|
| Benjamin D Malkin, MD | Icahns School of Medicine at Mount Sinai | Principal Investigator |
| Satish Govindaraj, MD | Icahn School of Medicine at Mount Sinai | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Icahn School of Medicine at Mount Sinai | New York | New York | 10029 | United States |
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Subjects were recruited from September 2014 to April 2016 at the Mount Sinai Department of Otolaryngology-Head & Neck Surgery rhinology practice.
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| ID | Title | Description |
|---|---|---|
| FG000 | Doxycycline | Doxycycline plus oral methylprednisolone and nasal saline sprays Doxycycline: Doxycycline (200 mg PO X 1 dose on Day 1, then 100 mg PO daily) for Day 2-20 methylprednisolone: oral methylprednisolone: 32 mg x 5 days, 16 mg x 5 days, 8 mg x 10 days nasal saline spray: nasal saline sprays: 2 sprays each nostril three times a day Flonase: daily nasal steroid sprays (Flonase, 2 sprays each nostril daily). |
| FG001 | Sugar Pill | placebo pill plus oral methylprednisolone for three weeks. After this, maintenance therapy which includes nasal saline sprays and daily nasal steroid sprays. methylprednisolone: oral methylprednisolone: 32 mg x 5 days, 16 mg x 5 days, 8 mg x 10 days Flonase: daily nasal steroid sprays (Flonase, 2 sprays each nostril daily). sugar pill: placebo pill to match doxycycline |
| Title | Milestones | Reasons Not Completed | ||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
|
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| ID | Title | Description |
|---|---|---|
| BG000 | Doxycycline | Doxycycline plus oral methylprednisolone and nasal saline sprays |
| BG001 | Sugar Pill | placebo pill plus oral methylprednisolone for three weeks. After this, maintenance therapy which includes nasal saline sprays and daily nasal steroid sprays. |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Mean |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Sino-nasal Outcome Test (SNOT 22) | a validated 22 item quality of life questionnaire for patients with chronic rhinosinusitis. Range of 0 to 110, higher scores indicate worse outcome | An additional 7 patients in the treatment group and 10 patients in the placebo group completed SNOT-22 scores via phone calls, even after study withdrawal. | Posted | Mean | Standard Deviation | units on a scale | Baseline and 12 weeks |
|
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Doxycycline | Doxycycline plus oral methylprednisolone and nasal saline sprays |
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Power not adequate and study is at risk for a Type II error - study was ended prior to complete sample size accrual. Study recruited high percentage of severe disease patients, thus did not accurately represent moderate disease patients.
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Dr. Benjamin Malkin | Icahn School of Medicine at Mount Sinai | Benjamin.D.Malkin@kp.org |
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| ID | Term |
|---|---|
| D004318 | Doxycycline |
| D008775 | Methylprednisolone |
| D000068298 | Fluticasone |
| D000073893 | Sugars |
| ID | Term |
|---|---|
| D013754 | Tetracyclines |
| D009279 | Naphthacenes |
| D011084 | Polycyclic Aromatic Hydrocarbons |
| D006841 | Hydrocarbons, Aromatic |
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| methylprednisolone | Drug | oral methylprednisolone: 32 mg x 5 days, 16 mg x 5 days, 8 mg x 10 days |
|
| nasal saline spray | Drug | nasal saline sprays: 2 sprays each nostril three times a day |
|
| Flonase | Drug | daily nasal steroid sprays (Flonase, 2 sprays each nostril daily). |
|
|
| sugar pill | Drug | placebo pill to match doxycycline |
|
|
| Baseline and 12 weeks |
| Middle Meatus Culture | Culture swab for the presence or absence of microbial growth | Baseline and 12 weeks |
| Subjective Symptom Composite Scoring | A subjective symptom score will be extracted from the patient's score (on a scale of 0-5, where 0 defines no problems with the given symptom and 5 defines maximal problems ) on the SNOT-22 for each fo the following symptoms: "blockage/congestion," "runny nose," "post-nasal discharge," "facial pain/pressure," and "sense of taste/smell." Range of 0 to 25, with higher score reflecting worse symptoms. | Baseline and 12 weeks |
| Visual Analog Scale | The visual analog scale for overall symptoms will be used to define disease severity. Range of 0 to 10. As per the European Position Paper 2012, mild, moderate, and severe disease will be defined as 0 to and including 3, > 3 to and including 7, and > 7 to and including 10, respectively. | Baseline and 12 weeks |
| BG002 | Total | Total of all reporting groups |
| years |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Number of Participants with Prior Endoscopic Sinus Surgery (ESS) | Count of Participants | Participants |
|
|
|
| Secondary | Endoscopic Nasal Polyp Score | 0- Absence of nasal polyps
| There were 12 subject withdrawals in the treatment group and 14 in the placebo group. | Posted | Mean | Standard Deviation | units on a scale | Baseline and 12 weeks |
|
|
|
| Secondary | Middle Meatus Culture | Culture swab for the presence or absence of microbial growth | Posted | Count of Participants | Participants | Baseline and 12 weeks |
|
|
|
| Secondary | Subjective Symptom Composite Scoring | A subjective symptom score will be extracted from the patient's score (on a scale of 0-5, where 0 defines no problems with the given symptom and 5 defines maximal problems ) on the SNOT-22 for each fo the following symptoms: "blockage/congestion," "runny nose," "post-nasal discharge," "facial pain/pressure," and "sense of taste/smell." Range of 0 to 25, with higher score reflecting worse symptoms. | There were 12 subject withdrawals in the treatment group and 14 in the placebo group. | Posted | Mean | Standard Deviation | units on a scale | Baseline and 12 weeks |
|
|
|
| Secondary | Visual Analog Scale | The visual analog scale for overall symptoms will be used to define disease severity. Range of 0 to 10. As per the European Position Paper 2012, mild, moderate, and severe disease will be defined as 0 to and including 3, > 3 to and including 7, and > 7 to and including 10, respectively. | There were 12 subject withdrawals in the treatment group and 14 in the placebo group. | Posted | Mean | Standard Deviation | units on a scale | Baseline and 12 weeks |
|
|
|
| 0 |
| 24 |
| 0 |
| 24 |
| 0 |
| 24 |
| EG001 | Sugar Pill | placebo pill plus oral methylprednisolone for three weeks. After this, maintenance therapy which includes nasal saline sprays and daily nasal steroid sprays. | 0 | 25 | 0 | 25 | 0 | 25 |
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| D006844 |
| Hydrocarbons, Cyclic |
| D006838 | Hydrocarbons |
| D009930 | Organic Chemicals |
| D011083 | Polycyclic Compounds |
| D011239 | Prednisolone |
| D011246 | Pregnadienetriols |
| D011245 | Pregnadienes |
| D011278 | Pregnanes |
| D013256 | Steroids |
| D000072473 | Fused-Ring Compounds |
| D000730 | Androstadienes |
| D000736 | Androstenes |
| D000731 | Androstanes |
| D002241 | Carbohydrates |
| 12 weeks |
|
|
| No growth initial visit, but growth at 12 weeks |
|
| 12 weeks |
|
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| 12 weeks |
|
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