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The Protective Effect of Ginkgo Biloba Extract on Cisplatin-induced Ototoxicity in Humans

Primary Purpose

Ototoxicity, Hearing Loss

Status
Completed
Phase
Phase 2
Locations
Brazil
Study Type
Interventional
Intervention
Ginkgo Biloba Extract (GBE761)
Placebo
Sponsored by
University of Brasilia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Ototoxicity focused on measuring Ear protection, Ginkgo Biloba Extract, Distortion-product otoacoustic emission, Ototoxicity, Cisplatin

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Over the age of eighteen
  • Patients that will begin treatment with cisplatin
  • No prior treatment with cisplatin

Exclusion Criteria:

  • Individuals with middle ear, cochlear or retrocochlear disease
  • Presence of changes in pure tone audiometry and/or distortion-product otoacoustic emissions

Sites / Locations

  • Hospital de Base do Distrito Federal (HBDF)

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Study Group

Control Group(CG)

Arm Description

The Study Group(SG) received Ginkgo biloba extract(GBE761)(240mg/day)plus cisplatin(CDDP)

The Control Group received Placebo plus CDDP

Outcomes

Primary Outcome Measures

the effect of GBE761 as a possible protector against cisplatin (CDDP) induced hearing loss was evaluated through the DPOAE. Comparisons were made between baseline measurements and those records after maximum cumulative CDDP dosage.
The protective effect of GBE761 on CDDP induced ototoxicity in human beings was evaluated with DPOAE mean amplitudes and signal-to-noise ratio (SNR) values at in the frequencies ranging from 1 to 8KHz in the study and control groups, between before and after cumulative CDDP injections, in order to evaluate the significant differences in DPOAE results, and so to differentiate hearing status ( normal hearing or hearing loss) while the subjects were taking GBE or placebo.

Secondary Outcome Measures

Full Information

First Posted
June 1, 2010
Last Updated
June 7, 2010
Sponsor
University of Brasilia
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1. Study Identification

Unique Protocol Identification Number
NCT01139281
Brief Title
The Protective Effect of Ginkgo Biloba Extract on Cisplatin-induced Ototoxicity in Humans
Official Title
The Protective Effect of Ginkgo Biloba Extract on Cisplatin-Induced Ototoxicity in Humans Beings Evaluated by Distortion Product Otoacoustic Emissions
Study Type
Interventional

2. Study Status

Record Verification Date
May 2010
Overall Recruitment Status
Completed
Study Start Date
June 2007 (undefined)
Primary Completion Date
June 2008 (Actual)
Study Completion Date
June 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
University of Brasilia

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The proposal of this study was to evaluate in human beings, using distortion product otoacoustic emission (DPOAE) test, the action of ginkgo biloba extract (GBE761)as a possible ear protective against cisplatin (CDDP) induced hearing loss.
Detailed Description
The ototoxicity is an alteration caused by drugs that compromises the auditory and vestibular functions. The cisplatin (CDDP) is a potent antineoplastic agent used for the treatment of cancer in both adults and children although it has several side effects. Current opinion is that cisplatin ototoxicity occurs due to alterations in the antioxidant system of the outer hair cells (OHC) of the cochlea. The distortion-product otoacoustic emissions (DPOAE) has been showed to be a sensitive test for diagnosis of OHC injury and has been used for monitoring treatment with ototoxic drugs. Because of their antioxidant properties, the ginkgo biloba extract (GBE761) was evaluated in human beings as a possible ear protective against cisplatin induced hearing loss, using DPOAE test.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ototoxicity, Hearing Loss
Keywords
Ear protection, Ginkgo Biloba Extract, Distortion-product otoacoustic emission, Ototoxicity, Cisplatin

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
15 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Study Group
Arm Type
Active Comparator
Arm Description
The Study Group(SG) received Ginkgo biloba extract(GBE761)(240mg/day)plus cisplatin(CDDP)
Arm Title
Control Group(CG)
Arm Type
Placebo Comparator
Arm Description
The Control Group received Placebo plus CDDP
Intervention Type
Drug
Intervention Name(s)
Ginkgo Biloba Extract (GBE761)
Other Intervention Name(s)
Study Group
Intervention Description
The subjects were randomized and allocated in two groups: Control Group(CG) and Study Group(SG). the study group received GBE761(120mg twice a day) plus cisplatin and was guided to ingest GBE761 just before initial cisplatin dosage. The maximum cumulative cisplatin dosage was 300mg/m². They were followed up for ninety days. Comparisons were made between baseline distortion-product otoacoustic emissions measurements and those DPOAE records after maximum cumulative cisplatin dosage.
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Control Group
Intervention Description
The subjects were randomized and allocated in two groups: control group and study group. The control group received placebo plus cisplatin and was guided to ingest Placebo just before initial cisplatin dosage. The maximum cumulative cisplatin dosage was 300mg/m². They were followed up for ninety days. Comparisons were made between baseline distortion-product otoacoustic emissions measurements and those DPOAE records after maximum cumulative cisplatin dosage.
Primary Outcome Measure Information:
Title
the effect of GBE761 as a possible protector against cisplatin (CDDP) induced hearing loss was evaluated through the DPOAE. Comparisons were made between baseline measurements and those records after maximum cumulative CDDP dosage.
Description
The protective effect of GBE761 on CDDP induced ototoxicity in human beings was evaluated with DPOAE mean amplitudes and signal-to-noise ratio (SNR) values at in the frequencies ranging from 1 to 8KHz in the study and control groups, between before and after cumulative CDDP injections, in order to evaluate the significant differences in DPOAE results, and so to differentiate hearing status ( normal hearing or hearing loss) while the subjects were taking GBE or placebo.
Time Frame
the patients were followed about ninety days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Over the age of eighteen Patients that will begin treatment with cisplatin No prior treatment with cisplatin Exclusion Criteria: Individuals with middle ear, cochlear or retrocochlear disease Presence of changes in pure tone audiometry and/or distortion-product otoacoustic emissions
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mirela A Dias
Organizational Affiliation
University of Brasilia
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Carlos CP Oliveira
Organizational Affiliation
University of Brasilia
Official's Role
Study Chair
Facility Information:
Facility Name
Hospital de Base do Distrito Federal (HBDF)
City
Brasília
State/Province
DF
ZIP/Postal Code
70000-000
Country
Brazil

12. IPD Sharing Statement

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The Protective Effect of Ginkgo Biloba Extract on Cisplatin-induced Ototoxicity in Humans

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