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Effect of Pilocarpine in Patients With Xerostomia

Primary Purpose

Xerostomia

Status
Unknown status
Phase
Phase 4
Locations
Brazil
Study Type
Interventional
Intervention
Pilocarpine
Spray without Pilocarpine
Sponsored by
University of Sao Paulo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Xerostomia focused on measuring Xerostomia, Pilocarpine, Quality of life

Eligibility Criteria

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

Inclusion Criteria:

  • Age equal or superior to 18 years;
  • Both genders;
  • Lucid and without diagnosis of any psychiatric disorder;
  • Diagnosed with head and neck cancer and treated for a period of up to 5 years with radiotherapy where the major salivary glands (parotid, submandibular and sublingual) were included in the radiation field;
  • Primary Sjögren's syndrome with the diagnosis made by the American-European criteria.

Exclusion Criteria:

  • Sensitivity to pilocarpine
  • Secondary Sjögren's syndrome;
  • Type II diabetes mellitus;
  • AIDS;
  • pregnant or lactating women;
  • Glaucoma;
  • Uncontrolled asthma;
  • Chronic obstructive pulmonary disease;
  • Renal diseases;
  • Severe cardiovascular diseases;
  • Gastrointestinal disorders;
  • Hepatic insufficiency.

Sites / Locations

  • University of São PauloRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Pilocarpine

Placebo

Arm Description

Spray with Pilocarpine

Spray without Pilocarpine

Outcomes

Primary Outcome Measures

Salivary flow
measured by stimulated salivation

Secondary Outcome Measures

Quality of life
measured by Oral Health Impact Profile (OHIP-14)
Xerostomia grade
measured by Xerostomia Inventory

Full Information

First Posted
November 27, 2016
Last Updated
November 30, 2016
Sponsor
University of Sao Paulo
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1. Study Identification

Unique Protocol Identification Number
NCT02982577
Brief Title
Effect of Pilocarpine in Patients With Xerostomia
Official Title
Effect of Pilocarpine in Patients With Xerostomia
Study Type
Interventional

2. Study Status

Record Verification Date
November 2016
Overall Recruitment Status
Unknown status
Study Start Date
April 2016 (undefined)
Primary Completion Date
June 2017 (Anticipated)
Study Completion Date
July 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Sao Paulo

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to evaluate the effectiveness of a spray the basis of pilocarpine on salivary flow of patients with xerostomia, by radiation therapy, and primary Sjögren's Syndrome treated at the Clinics Hospital of Faculty of Medicine of Ribeirão Preto (HCFMRP-USP), and its impact on quality of life.
Detailed Description
There will be two groups: Group 1 (G1) - will use a spray with pilocarpine for three months and after a washout period of a month, use a spray without pilocarpine for another three months; Group 2 (G2) - will use a spray without pilocarpine for three months and after a washout period of a month, use a spray with pilocarpine for another three months (in a randomized, controlled, duble blind and crossover study). Participants will be submitted to OHIP-14, Xerostomia Inventory (XI) and salivary flow measurement before the start of therapy - baseline (T0), one (T2), two (T3) and three (T4) months after starting the use of spray, after washout, crossover occurs and the same parameters are measured for the same periods (T0', T2', T3' and T4'), and is measured one hour after the saliva (T1 and T1') baseline.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Xerostomia
Keywords
Xerostomia, Pilocarpine, Quality of life

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Pilocarpine
Arm Type
Experimental
Arm Description
Spray with Pilocarpine
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Spray without Pilocarpine
Intervention Type
Drug
Intervention Name(s)
Pilocarpine
Other Intervention Name(s)
Pilocarpine spray
Intervention Description
Spray the basis of 1.54% pilocarpine, 3 times per day (each 8 hours), during 90 days.
Intervention Type
Other
Intervention Name(s)
Spray without Pilocarpine
Other Intervention Name(s)
Placebo
Intervention Description
Spray without pilocarpine, 3 times per day (each 8 hours), during 90 days.
Primary Outcome Measure Information:
Title
Salivary flow
Description
measured by stimulated salivation
Time Frame
baseline, 1 hour after baseline and each 30 days up to 90 days until start the wash out, and after crossover will repeat these time frame measures
Secondary Outcome Measure Information:
Title
Quality of life
Description
measured by Oral Health Impact Profile (OHIP-14)
Time Frame
baseline and each 30 days up to 90 days until start the wash out, and after crossover will repeat these time frame measures
Title
Xerostomia grade
Description
measured by Xerostomia Inventory
Time Frame
baseline and each 30 days up to 90 days until start the wash out, and after crossover will repeat these time frame measures

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age equal or superior to 18 years; Both genders; Lucid and without diagnosis of any psychiatric disorder; Diagnosed with head and neck cancer and treated for a period of up to 5 years with radiotherapy where the major salivary glands (parotid, submandibular and sublingual) were included in the radiation field; Primary Sjögren's syndrome with the diagnosis made by the American-European criteria. Exclusion Criteria: Sensitivity to pilocarpine Secondary Sjögren's syndrome; Type II diabetes mellitus; AIDS; pregnant or lactating women; Glaucoma; Uncontrolled asthma; Chronic obstructive pulmonary disease; Renal diseases; Severe cardiovascular diseases; Gastrointestinal disorders; Hepatic insufficiency.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Raony MS Pereira, MSc
Phone
+55 16 981275221
Email
raonymolimsp@hotmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Ana CF Motta, PhD
Phone
+55 16 33154067
Email
anacfm@usp.br
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Camila Tirapelli, PhD
Organizational Affiliation
University of São Paulo
Official's Role
Study Director
Facility Information:
Facility Name
University of São Paulo
City
Ribeirao Preto
State/Province
São Paulo
ZIP/Postal Code
14040904
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Raony MS Pereira, MSc
Phone
+55 16 981275221
Email
raonymolimsp@hotmail.com
First Name & Middle Initial & Last Name & Degree
Ana CF Motta, PhD
Phone
+55 16 33154067
Email
anacfm@usp.br

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
26436597
Citation
Davies AN, Thompson J. Parasympathomimetic drugs for the treatment of salivary gland dysfunction due to radiotherapy. Cochrane Database Syst Rev. 2015 Oct 5;2015(10):CD003782. doi: 10.1002/14651858.CD003782.pub3.
Results Reference
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PubMed Identifier
25322971
Citation
Hanchanale S, Adkinson L, Daniel S, Fleming M, Oxberry SG. Systematic literature review: xerostomia in advanced cancer patients. Support Care Cancer. 2015 Mar;23(3):881-8. doi: 10.1007/s00520-014-2477-8. Epub 2014 Oct 18.
Results Reference
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PubMed Identifier
24176001
Citation
Nikles J, Mitchell GK, Hardy J, Agar M, Senior H, Carmont SA, Schluter PJ, Good P, Vora R, Currow D. Do pilocarpine drops help dry mouth in palliative care patients: a protocol for an aggregated series of n-of-1 trials. BMC Palliat Care. 2013 Oct 31;12(1):39. doi: 10.1186/1472-684X-12-39.
Results Reference
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PubMed Identifier
23346917
Citation
Brito-Zeron P, Siso-Almirall A, Bove A, Kostov BA, Ramos-Casals M. Primary Sjogren syndrome: an update on current pharmacotherapy options and future directions. Expert Opin Pharmacother. 2013 Feb;14(3):279-89. doi: 10.1517/14656566.2013.767333. Epub 2013 Jan 25.
Results Reference
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PubMed Identifier
27767109
Citation
Spivakovsky S, Spivakovsky Y. Parasympathomimetic drugs for dry mouth due to radiotherapy. Evid Based Dent. 2016 Sep;17(3):79. doi: 10.1038/sj.ebd.6401185.
Results Reference
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PubMed Identifier
26867879
Citation
Yang WF, Liao GQ, Hakim SG, Ouyang DQ, Ringash J, Su YX. Is Pilocarpine Effective in Preventing Radiation-Induced Xerostomia? A Systematic Review and Meta-analysis. Int J Radiat Oncol Biol Phys. 2016 Mar 1;94(3):503-11. doi: 10.1016/j.ijrobp.2015.11.012. Epub 2015 Nov 10.
Results Reference
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PubMed Identifier
26563850
Citation
Cheng CQ, Xu H, Liu L, Wang RN, Liu YT, Li J, Zhou XK. Efficacy and safety of pilocarpine for radiation-induced xerostomia in patients with head and neck cancer: A systematic review and meta-analysis. J Am Dent Assoc. 2016 Apr;147(4):236-43. doi: 10.1016/j.adaj.2015.09.014. Epub 2015 Nov 10.
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PubMed Identifier
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Citation
Nikles J, Mitchell GK, Hardy J, Agar M, Senior H, Carmont SA, Schluter PJ, Good P, Vora R, Currow D. Testing pilocarpine drops for dry mouth in advanced cancer using n-of-1 trials: A feasibility study. Palliat Med. 2015 Dec;29(10):967-74. doi: 10.1177/0269216315585473. Epub 2015 May 22.
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PubMed Identifier
25841622
Citation
Wong RK, Deshmukh S, Wyatt G, Sagar S, Singh AK, Sultanem K, Nguyen-Tan PF, Yom SS, Cardinale J, Yao M, Hodson I, Matthiesen CL, Suh J, Thakrar H, Pugh SL, Berk L. Acupuncture-Like Transcutaneous Electrical Nerve Stimulation Versus Pilocarpine in Treating Radiation-Induced Xerostomia: Results of RTOG 0537 Phase 3 Study. Int J Radiat Oncol Biol Phys. 2015 Jun 1;92(2):220-7. doi: 10.1016/j.ijrobp.2015.01.050. Epub 2015 Apr 1.
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PubMed Identifier
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Citation
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Citation
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Citation
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Effect of Pilocarpine in Patients With Xerostomia

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