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New Therapy of Laryngeal Papilloma In Children

Primary Purpose

Papilloma

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
diindolylmethane (DIM)
585 nm pulsed dye laser
Sponsored by
Boston University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Papilloma focused on measuring papilloma, PDL, diindolylmethane, recurrence

Eligibility Criteria

10 Years - 21 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. 10 to 21 years of age
  2. laryngeal papillomas requiring surgical treatment
  3. willingness to participate in the study
  4. a signed informed consent form by guardian or parent

Exclusion Criteria:

  1. age less than 10 year old, or older than 21 year
  2. guardian or parent does not understand or can not sign the consent form
  3. malignant diseases such as laryngeal cancer
  4. history of being hypersensitive to cabbage or other cruciferous vegetables
  5. pregnancy

Sites / Locations

  • Boston Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

PDL+DIM pill

PDL+placebo pill

Arm Description

once-time 585 nm pulsed dye laser (PDL) treatment on the lesions, immediately followed by 3-month oral taking diindolylmethane (DIM, at 1.2-1.75mg/kg/day), in 15 subjects

once-time PDL treatment on the lesions, then followed by 3-month oral taking DIM placebo, in other 15 subjects

Outcomes

Primary Outcome Measures

Number of Cases With Recurrence of Laryngeal Papilloma in 5 Months
vocal lesion size and area after 5 month with surgery visible lesion found in >50% of the treated tissue area, after surgery

Secondary Outcome Measures

Estradiol Level in Blood Pre Treatment
determine side-effect by comparing Estradiol level in blood before and after treatment
Estradiol Level in Blood Post Treatment
determine side-effect by comparing Estradiol level in blood before and after treatment

Full Information

First Posted
December 31, 2007
Last Updated
May 16, 2017
Sponsor
Boston University
Collaborators
National Institute on Deafness and Other Communication Disorders (NIDCD)
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1. Study Identification

Unique Protocol Identification Number
NCT00591305
Brief Title
New Therapy of Laryngeal Papilloma In Children
Official Title
Voice Preserving Therapy of Laryngeal Papilloma In Children
Study Type
Interventional

2. Study Status

Record Verification Date
May 2017
Overall Recruitment Status
Terminated
Why Stopped
insufficient resource for recruitment
Study Start Date
September 2007 (undefined)
Primary Completion Date
August 2011 (Actual)
Study Completion Date
October 2011 (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
Yes

5. Study Description

Brief Summary
This study will determine efficacy of a new and combined treatment of laryngeal recurrent respiratory papillomatosis (RRP), by using a 585 nm pulsed dye laser (PDL) and a dietary supplement, diindolylmethane (DIM). We will compare this new treatment with PDL-only, in a total of 30 children (15 of each treatment), to determine whether this combined treatment would be effective and safe in preventing the RRP recurrence. This is the first study to combine PDL technique with DIM, to develop a new, voice-preserving and long-term effective method of managing laryngeal RRP in children.
Detailed Description
Previous studies have demonstrated that PDL can be used to remove lesions on the vocal cords and elsewhere in the throat causing less damage to surface tissues than other commonly used lasers. In our proposed clinical study, we seek to compare treatment efficacy for RRP by combining PDL with DIM, versus PDL-only treatment, in a total of 30 children with laryngeal papilloma. We will determine whether this combined treatment would be effective and safe in preventing or delaying the RRP recurrence while preserving voice quality. 30 children will be divided randomly into two treatment groups, 15 in each. The experimental group will receive one-time PDL treatment, followed by 3-month oral administration of DIM and an additional 12 months with no treatment. The other group will be treated with PDL-only, as a control, and take a placebo pill for 3 months. All of the patients will be followed for a total of 15 months. We will compare lesion recurrence and laboratory tests between the two groups, to determine efficacy and safety of the new treatment. This is the first study to combine new PDL laser technique with DIM, to develop a new, voice-preserving and long-term effective method of managing laryngeal RRP in children.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Papilloma
Keywords
papilloma, PDL, diindolylmethane, recurrence

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
laser only vs laser+ a dietary agent (DIM)
Masking
Participant
Masking Description
treatment to be selected based on a randomized number table, blinded to participants
Allocation
Randomized
Enrollment
1 (Actual)

8. Arms, Groups, and Interventions

Arm Title
PDL+DIM pill
Arm Type
Experimental
Arm Description
once-time 585 nm pulsed dye laser (PDL) treatment on the lesions, immediately followed by 3-month oral taking diindolylmethane (DIM, at 1.2-1.75mg/kg/day), in 15 subjects
Arm Title
PDL+placebo pill
Arm Type
Placebo Comparator
Arm Description
once-time PDL treatment on the lesions, then followed by 3-month oral taking DIM placebo, in other 15 subjects
Intervention Type
Dietary Supplement
Intervention Name(s)
diindolylmethane (DIM)
Intervention Description
3-month DIM
Intervention Type
Device
Intervention Name(s)
585 nm pulsed dye laser
Intervention Description
once-time PDL
Primary Outcome Measure Information:
Title
Number of Cases With Recurrence of Laryngeal Papilloma in 5 Months
Description
vocal lesion size and area after 5 month with surgery visible lesion found in >50% of the treated tissue area, after surgery
Time Frame
Recurrence of pailloma at 5 months
Secondary Outcome Measure Information:
Title
Estradiol Level in Blood Pre Treatment
Description
determine side-effect by comparing Estradiol level in blood before and after treatment
Time Frame
Before treatment at baseline
Title
Estradiol Level in Blood Post Treatment
Description
determine side-effect by comparing Estradiol level in blood before and after treatment
Time Frame
5 month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 10 to 21 years of age laryngeal papillomas requiring surgical treatment willingness to participate in the study a signed informed consent form by guardian or parent Exclusion Criteria: age less than 10 year old, or older than 21 year guardian or parent does not understand or can not sign the consent form malignant diseases such as laryngeal cancer history of being hypersensitive to cabbage or other cruciferous vegetables pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Zhi Wang, MD
Organizational Affiliation
Boston University
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

Plan to Share IPD
No
IPD Sharing Plan Description
no such meaningful data available due to insufficient recruitment

Learn more about this trial

New Therapy of Laryngeal Papilloma In Children

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