Viewing Study NCT00319670



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Last Modification Date: 2024-10-26 @ 9:24 AM
Study NCT ID: NCT00319670
Status: COMPLETED
Last Update Posted: 2013-02-07
First Post: 2006-04-27

Brief Title: A Pilot Study of a New MiraLax Dose Formulation For Use in Constipated Children
Sponsor: Braintree Laboratories
Organization: Braintree Laboratories

Study Overview

Official Title: A Pilot Study of a New MiraLax Dose Formulation For Use in Constipated Children
Status: COMPLETED
Status Verified Date: 2013-02
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: To evaluate patient acceptance of a new MiraLax dose formulation in children currently treated with polyethylene glycol 3350 powder for treatment of constipation
Detailed Description: To evaluate patient acceptance of a new MiraLax dose formulation in children currently treated with polyethylene glycol 3350 powder for treatment of constipation

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None