Celebrex (Celecoxib) Treatment of Laryngeal Papilloma
Primary Purpose
Laryngeal Papilloma
Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Celebrex
PDL
CO2 laser or microsurgery
Sponsored by
About this trial
This is an interventional treatment trial for Laryngeal Papilloma focused on measuring Papilloma, pulsed dye laser, Celebrex, voice
Eligibility Criteria
Inclusion Criteria:
- 18 to 64 years of age
- with laryngeal papillomas requiring surgical treatment
- willingness to participate in the study
- a signed informed consent form
Exclusion Criteria:
- age less than 18 years
- evidence of mental impairment so that the patient can not understand or sign the consent form
- malignant diseases such as laryngeal cancer
- established coronary heart and artery disorder, cerebrovascular disease, and other cardiovascular diseases
- established diabetes, which requires (1) insulin treatment; or (2) more than 2 oral agents of medication; or (3) to have a baseline HgbA1c >8.0
- hypertension, with ongoing blood pressure > 150 mg Hg systolic or to require medication
- family history with serious cardiovascular events and problems
- any sign and evidence which in the opinion of cardiovascular physician warrants exclusion of subject
Sites / Locations
- Boston Medical Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
PDL+Celebrex
standard surgery
Arm Description
endoscopic treatment with once-time PDL radiation at 6.0-8.0 J on laryngeal papilloma, followed by oral taking of 9-month Celebrex (100mg, BID), in 15 subjects
once-time and routine surgery, with either of carbon dioxide (CO2) laser radiation at 10.0-20.0 W or "cold" surgery with microinstruments, in 15 subjects
Outcomes
Primary Outcome Measures
Number of Case With Papilloma Recurrence During a 12-month Follow up
Criteria for the recurrence: the site scoring >4, plus visible lesion found in >50% of the treated tissue area, after surgery Description: The caculation of the site scoring is based on a called Derkay's scoring system: to indicate how many anatomic site involved, from the 0 (the best)to 13 (the worst),among a total of 13 laryngeal sites such as epiglottis or right true vocal cords.
Secondary Outcome Measures
Time Course (Month) With Papilloma Recurrence During 12-month Follow up
The measuer is reported as time course (i.e., how many month) to see papilloma recurrence if there is any such recurrence.
Full Information
NCT ID
NCT00592319
First Posted
December 31, 2007
Last Updated
August 24, 2012
Sponsor
Boston University
Collaborators
National Institute on Deafness and Other Communication Disorders (NIDCD)
1. Study Identification
Unique Protocol Identification Number
NCT00592319
Brief Title
Celebrex (Celecoxib) Treatment of Laryngeal Papilloma
Official Title
Voice-preserving Treatment of Laryngeal Papilloma
Study Type
Interventional
2. Study Status
Record Verification Date
August 2012
Overall Recruitment Status
Terminated
Why Stopped
03/01/2009,due to date close to termination of this funding/study period
Study Start Date
May 2005 (undefined)
Primary Completion Date
July 2009 (Actual)
Study Completion Date
July 2009 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Boston University
Collaborators
National Institute on Deafness and Other Communication Disorders (NIDCD)
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Respiratory recurrent papilloma (RRP) is one of the most common benign tumors. Surgical removal is the current management for RRP, but it is a very traumatic procedure, and often leads to permanent voice dysfunction. In this study, we will develop a new, combined RRP treatment with a pulsed dye laser (PDL) and Celebrex. We will determine if Celebrex, a newly developed inhibitor of cyclooxygenase (COX)-2, can provide a long-term inhibitory effect on RRP, therefore preventing RRP from recurring. This combined strategy, if successful in this proposed study, will provide a new and ideal "voice-preserving" therapy for RRP that will deliver long-term efficacy in managing RRP.
Detailed Description
RRP and its surgeries usually involves the vocal cords or other regions of the larynx, thereby, resulting in a poor voice. Our previous studies have shown the efficacy and safety of a microvascular targeting technique (MVT) for RRP treatment using the 585 nm PDL. This technique provides a less traumatic alternative to surgery. However, postoperative recurrence of lesions still remains a problem because of microvascular regrowth. This study is a continuation of our effort to develop a new and less traumatic treatment for RRP. In this study, we will develop a new, combined RRP treatment with PDL and Celebrex. We will determine if Celebrex, a newly developed inhibitor of COX-2, can provide a long-term inhibitory effect on RRP through its anti-angiogenic activity and the synergic effect produced with the laser therapy. The hypothesis is that postoperative administration of Celebrex will provide a long-term inhibitory effect on microvascular regrowth and on COX-2 enzyme, thereby, preventing RRP from recurring after the PDL therapy. Our specific aim in this study is to determine the synergic effect between PDL and Celebrex and long-term efficacy of Celecoxib in preventing postoperative RRP recurrence. We will compare this new combined strategy with traditional treatments in 30 adult patients. This is the first time to combined this new laser MVT technique with a COX-2 inhibitor for microvascular targeting therapy of RRP. This combined strategy, if successful in this proposed study, will provide a new and ideal "voice-preserving" therapy for RRP that will deliver long-term efficacy in managing RRP and will be safe and convenient enough for use in out-patient treatment.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Laryngeal Papilloma
Keywords
Papilloma, pulsed dye laser, Celebrex, voice
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
10 (Actual)
8. Arms, Groups, and Interventions
Arm Title
PDL+Celebrex
Arm Type
Experimental
Arm Description
endoscopic treatment with once-time PDL radiation at 6.0-8.0 J on laryngeal papilloma, followed by oral taking of 9-month Celebrex (100mg, BID), in 15 subjects
Arm Title
standard surgery
Arm Type
Active Comparator
Arm Description
once-time and routine surgery, with either of carbon dioxide (CO2) laser radiation at 10.0-20.0 W or "cold" surgery with microinstruments, in 15 subjects
Intervention Type
Drug
Intervention Name(s)
Celebrex
Other Intervention Name(s)
Celecoxib
Intervention Description
oral taking of Celebrex (100 mg, BID) for 9 months
Intervention Type
Device
Intervention Name(s)
PDL
Other Intervention Name(s)
585 nm PDL (cynosure Inc. Mass)
Intervention Description
once time radiation on laryngeal papilloma with PDL , at 6.0-8.0 J
Intervention Type
Procedure
Intervention Name(s)
CO2 laser or microsurgery
Other Intervention Name(s)
ablation laser or micro-instrumental surgery
Intervention Description
once-time surgery to remove laryngeal papilloma
Primary Outcome Measure Information:
Title
Number of Case With Papilloma Recurrence During a 12-month Follow up
Description
Criteria for the recurrence: the site scoring >4, plus visible lesion found in >50% of the treated tissue area, after surgery Description: The caculation of the site scoring is based on a called Derkay's scoring system: to indicate how many anatomic site involved, from the 0 (the best)to 13 (the worst),among a total of 13 laryngeal sites such as epiglottis or right true vocal cords.
Time Frame
12-month follow up
Secondary Outcome Measure Information:
Title
Time Course (Month) With Papilloma Recurrence During 12-month Follow up
Description
The measuer is reported as time course (i.e., how many month) to see papilloma recurrence if there is any such recurrence.
Time Frame
12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
64 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
18 to 64 years of age
with laryngeal papillomas requiring surgical treatment
willingness to participate in the study
a signed informed consent form
Exclusion Criteria:
age less than 18 years
evidence of mental impairment so that the patient can not understand or sign the consent form
malignant diseases such as laryngeal cancer
established coronary heart and artery disorder, cerebrovascular disease, and other cardiovascular diseases
established diabetes, which requires (1) insulin treatment; or (2) more than 2 oral agents of medication; or (3) to have a baseline HgbA1c >8.0
hypertension, with ongoing blood pressure > 150 mg Hg systolic or to require medication
family history with serious cardiovascular events and problems
any sign and evidence which in the opinion of cardiovascular physician warrants exclusion of subject
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wang Zhi, M.D
Organizational Affiliation
Boston Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Boston Medical Center
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02118
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Celebrex (Celecoxib) Treatment of Laryngeal Papilloma
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