NIPH Clinical Trials Search

JAPANESE
国立保健医療科学院
UMIN ID: UMIN000005276

Registered date:01/04/2011

Efficacy and safety of Oral pirocarpin for xerostomia patients.

Basic Information

Recruitment status Complete: follow-up complete
Health condition(s) or Problem(s) studiedxerostomia
Date of first enrollment2011/04/01
Target sample size40
Countries of recruitmentJapan
Study typeInterventional
Intervention(s)5mg of oral pilocarpine three times daily 24 weeks follow up

Outcome(s)

Primary OutcomeQuantity of the stimulated saliva Level of oral moisture measured by a moisture checker
Secondary Outcome

Key inclusion & exclusion criteria

Age minimum20years-old
Age maximumNot applicable
GenderMale and Female
Include criteriaxerostomia patients
Exclude criteriaContraindication to oral pilocarpine. Pregnancy or women with suspected pregnancy. The patients who could not be provided with informed consent. Unsuitability for the trial based on clinical judgement.

Related Information

Contact

public contact
Name Yumiko Ohbayashi
Address 1750-1 Ikenobe, Miki-cho, Kita-gun, Kagawa Prefecture Japan
Telephone 087-891-2227
E-mail
Affiliation Kagawa University Department of Oral and Maxillofacial Surgery
scientific contact
Name Yumiko Ohbayashi
Address 1750-1 Ikenobe, Miki-cho, Kita-gun, Kagawa Prefecture Japan
Telephone 087-891-2227
E-mail
Affiliation Kagawa University Department of Oral and Maxillofacial Surgery