ClinicalTrials.Veeva

Menu

Celebrex (Celecoxib) Treatment of Laryngeal Papilloma

Boston University logo

Boston University

Status and phase

Terminated
Phase 2

Conditions

Laryngeal Papilloma

Treatments

Procedure: CO2 laser or microsurgery
Device: PDL
Drug: Celebrex

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT00592319
R01DC006617 (U.S. NIH Grant/Contract)
RDC-006617A

Details and patient eligibility

About

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.

Full 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.

Enrollment

10 patients

Sex

All

Ages

18 to 64 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. 18 to 64 years of age
  2. with laryngeal papillomas requiring surgical treatment
  3. willingness to participate in the study
  4. a signed informed consent form

Exclusion criteria

  1. age less than 18 years
  2. evidence of mental impairment so that the patient can not understand or sign the consent form
  3. malignant diseases such as laryngeal cancer
  4. established coronary heart and artery disorder, cerebrovascular disease, and other cardiovascular diseases
  5. 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
  6. hypertension, with ongoing blood pressure > 150 mg Hg systolic or to require medication
  7. family history with serious cardiovascular events and problems
  8. any sign and evidence which in the opinion of cardiovascular physician warrants exclusion of subject

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

10 participants in 2 patient groups

PDL+Celebrex
Experimental group
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
Treatment:
Drug: Celebrex
Device: PDL
standard surgery
Active Comparator group
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
Treatment:
Procedure: CO2 laser or microsurgery

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems