The Efficacy Of Diclectin® For Nausea And Vomiting Of Pregnancy

Nausea and Vomiting of Pregnancy Clinical Trial

Official title:

A Double-Blind, Multicenter, Randomized, Placebo-Controlled Trial Of The Efficacy Of Diclectin® For Nausea And Vomiting Of Pregnancy

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00614445
• Other study ID #: DIC-301
• Status: Completed
• Phase: Phase 3
• Start date: January 2008
• Est. completion date: December 2009

Study information

• Verified date: August 2011
• Source: Duchesnay Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to determine whether Diclectin® (doxylamine succinate USP 10 mg and pyridoxine HCl 10 mg) is more effective at controlling the nausea and vomiting of pregnancy than a placebo.

Description:

Nausea and vomiting of pregnancy (NVP), also known as "morning sickness," is a common condition that affects a large percentage of pregnant women. The symptoms can range from mild nausea to severe nausea and vomiting for which a woman may need to be hospitalized. Nausea and vomiting of pregnancy can affect a woman's quality of life and ability to conduct daily activities.

Diclectin® is a combination of 10 mg doxylamine succinate (an antihistamine), and 10 mg pyridoxine hydrochloride (vitamin B6) in a delayed release tablet formulation. It has been commercially available in Canada for the management of NVP for over 25 years and has been prescribed to over 33 million pregnant women.

Presently, there is no Food Drug and Administration (FDA) approved drug on the market to treat the symptoms of NVP. This study will test the efficacy of Diclectin® (doxylamine 10 mg, pyridoxine 10 mg in a delayed-release formulation) for NVP.

Patients enrolled in the study will receive between 2 and 4 tablets of Diclectin® or placebo daily, depending on their symptoms for up to 14 days. Patients will assess their symptoms of nausea and vomiting daily using a standardized questionnaire.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 280
• Est. completion date: December 2009
• Est. primary completion date: July 2009
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• The patient has signed a written informed consent to participate in the study and has agreed to follow dosing instructions and complete all required study visits.

• The patient is a pregnant female age equal to or greater than 18 years old.

• The patient's entry ultrasound indicates a viable pregnancy and confirms gestational age of the fetus is 7-14 weeks at the anticipated time of the first dose of study medication or placebo. If an ultrasound was done within 4 weeks of the admission visit, and results can be obtained, an additional ultrasound is not necessary.

• The patient is suffering from NVP and has a Pregnancy Unique Quantification of Emesis (PUQE) score =6.

• The patient has not responded to conservative management consisting of dietary/lifestyle advice according to the 2004 ACOG Practice Bulletin.

• The patient agrees, if on a multivitamin, to continue on their current dose of multivitamin for the duration of the trial.

• The patient does not plan termination of the pregnancy.

Exclusion Criteria:

• The investigator confirms the patient's nausea and vomiting is of etiology other than Nausea and Vomiting of Pregnancy (NVP).

• The patient has gestational trophoblastic disease or multifetal gestation.

• The patient has a condition for which antihistamines, in the opinion of the investigator, are contraindicated (epilepsy, alcoholism, glaucoma, chronic lung disease, urinary retention, heart block, etc.).

• The patient has used antihistamines, anticholinergics, dopamine antagonists, serotonin antagonists, ginger, or anti-emetic therapy (including acupressure, acupuncture, homeopathic remedies, medical hypnosis, relief bands etc) to treat NVP in the previous 48 hours or plans to do so during the study .

• The patient is using drugs that have anticholinergic activity (e.g., tricyclic antidepressants).

• The patient is taking multivitamins containing more than 10 mg of vitamin B6, or plans to do so during the study.

• The patient is taking supplementary vitamin B6 in addition to any multivitamin preparation, or plans to do so during the study.

• The patient is currently drinking any amount of alcohol.

• The patient has any condition that might interfere with the conduct of the study.

• The patient is likely to be unable to comply with study procedures because of inadequate cognitive skills.

• The patient has received an investigational drug within 30 days before enrollment in this study or is scheduled to receive an investigational drug during the course of this study.

Related Conditions & MeSH terms

• Nausea
• Nausea and Vomiting of Pregnancy
• Pregnancy Complications
• Vomiting

Intervention

Drug:
• doxylamine succinate 10 mg/pyridoxine hydrochloride 10 mg
up to 4 tablets daily, titrated according to the protocol
• Placebo
2 to 4 tablets daily titrated according to the protocol

Locations

Country	Name	City	State
United States	National Naval Medical Center	Bethesda	Maryland
United States	University of Texas Medical Branch	Galveston	Texas
United States	UTMB Pasadena Clinic	Pasadena	Texas
United States	UTMB Regional Maternal & Child Health Program--Pearland Clinic	Pearland	Texas
United States	Magee-Womens Hospital of University of Pittsburgh Medical Center	Pittsburgh	Pennsylvania
United States	Georgetown University Hospital	Washington	District of Columbia
United States	Washington Hospital Center Physicians	Washington	District of Columbia

Sponsors (2)

Lead Sponsor	Collaborator
Duchesnay Inc.	Premier Research Group plc

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Diclectin Versus Placebo for Treatment of Nausea and Vomiting of Pregnancy (NVP) as Measured by the Change in Pregnancy Unique-Quantification of Emesis (PUQE) Overall Score of Symptoms From Baseline (Day 1) to End of Study Visit (Day 15).	The objective of this double-blind, randomized, placebo-controlled study was to assess the efficacy, safety, and tolerability of oral Diclectin® in the treatment of nausea and vomiting of pregnancy (NVP) as measured by the Pregnancy Unique-Quantification of Emesis (PUQE) overall score of symptoms from baseline (Day 1) to end of study visit (Day 15). The PUQE score measured hours of nausea, number of times vomiting, and number of times retching for a TOTAL overall score of symptoms on a scale rated from 3 (no symptoms) to 15 (most severe).	Baseline (Day 1) to End of Study Visit Day 15 (± 1 day)